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Journal articles on the topic 'Erythematous'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

Chinnusamy, Manokaran, Ram Arvind Viswanathan, Sathiyanarayanan Janakiraman, and Roshna Elayidath. "Drug-Induced Lupus Erythematosus Associated with Proton Pump Inhibitor." Journal of Health and Allied Sciences NU 10, no. 03 (2020): 132–34. http://dx.doi.org/10.1055/s-0040-1716601.

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AbstractDrug-induced lupus erythematosus is an autoimmune phenomenon where the drug exposure leads to the development of systemic lupus erythematous like clinical features. Drug-induced lupus erythematosus can be divided into systemic lupus erythematous, subacute cutaneous lupus erythematous, and chronic cutaneous lupus erythematous. Here, we report a case of a 29-year-old female presented with systemic lupus erythematous due to chronic use of proton pump inhibitors, which is considered to be very rare.

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2

Cahyawari, Dartri, Eva K. Sutedja, Unwati Sugiri, Hendra Gunawan, and Oki Suwarsa. "An unusual case of pemphigus erythematosus." Case Reports in Clinical Pathology 4, no. 4 (2017): 14. http://dx.doi.org/10.5430/crcp.v4n4p14.

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Pemphigus erythematosus is characterized by fragile vesicles or bullae, erosions, crusts, and scales in seborrheic area. There are several forms of atypical lesions such as erythematous papules and plaques, verrucous plaques, pustules, and lichenification. Here, we report an atypical pemphigus erythematosus with erythematous papules, plaques, and pustules skin lesions. A 52-year-old Indonesian man presented with prominent pruritic erythematous macules, papules, plaques on the scalp, trunk, and extremities, and also a pustule for each on the back and right arm. Clinically, the patient was diagn

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3

Garbelini-Lima, Cleide, Gabriela Evangelista de Almeida, Sidharta Quércia Gabdelha, Andrea Cavalcante de Souza, Mara Lúcia Gomes de Souza, and Virginia Vilasboas Figueiras. "Discoid Lupus Erythematosus of the Scalp in a Patient with Systemic Lupus Erythematosus: A Case Report with Complete Hair Regrowth." Journal of the Portuguese Society of Dermatology and Venereology 79, no. 2 (2021): 155–58. http://dx.doi.org/10.29021/spdv.79.2.1283.

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Scalp involvement with hair loss is common in systemic lupus erythematosus. Discoid lupus erythematosus may cause scarring alopecia, characterized by well-delimited erythematous plaques with scales, follicular hyperkeratosis and atrophy, which is considered a trichological emergency. Early diagnosis and treatment are necessary in order to prevent permanent hair loss. We describe a 44 years’ old female patient with systemic lupus erythematosus for 4 years, with multiple areas of occipitoparietal alopecia, erythematous plaques, atrophy, scales and some bloody crusts. Trichoscopy, histopathology

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Shenoy, Manjunath M., Goutham Kilaru, Ashmiya Razak, and Malcolm Pinto. "Atypical dermatophytosis in a case of systemic lupus erythematosus." Our Dermatology Online 11, e (2020): e165.1-e165.3. http://dx.doi.org/10.7241/ourd.2020e.165.

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Systemic lupus erythematosus (SLE) is a multiorgan autoimmune connective tissue disease with many muco-cutaneous manifestations. We report a case of SLE on treatment presented with scaly erythematous plaques on the trunk and extremities and diffuse scaly erythematous macular lesions on the face resembling cutaneous lupus erythematosus. Laboratory evaluation established a diagnosis of tinea corporis with faciei. He responded to long term itraconazole therapy. This case focuses on the modification of tinea in an autoimmune disorder on immunosuppressive therapy and its therapeutic implications.

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Antonova, O. V., P. N. Trofimov, I. E. Belousova, and A. V. Samtsov. "Reticular erythematous mucinosis." Vestnik dermatologii i venerologii 90, no. 5 (2014): 96–99. http://dx.doi.org/10.25208/0042-4609-2014-90-5-96-99.

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This article presents modern data related to the clinical picture, pathologic features and treatment options of reticular erythematous mucinosis (REM). There is an opinion that REM, lupus erythematosus tumidus and Jessner - Kanof lymphocytic infiltration of the skin are similar nosological forms.

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Khabba, Chaimae Ait, Basma Karrakchou, Marwa Asermouh, Laila Berbich, Kaoutar Znati, and Karima Senouci. "Comedonal variant of chronic cutaneous lupus erythematosus on the nose." Our Dermatology Online 14, no. 3 (2023): 298–300. http://dx.doi.org/10.7241/ourd.20233.14.

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A thirty-year-old patient presented with an erythematous papule on the left nostril evolving for ten months. A clinical examination revealed an infiltrated, erythematous, well-limited plaque with a raised border, covered with multiple open and closed comedones. On dermoscopy, there was an erythematous background with some fine telangiectasias and horny plugs at the follicular orifices. A skin biopsy was performed, revealing orthokeratotic hyperkeratosis sinking into the follicular orifices dilated by sebum clumps with basal vacuolation associated with a subepidermal and periadnexal/perivascula

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7

Garcia, Brianae, Anis Hasnaoui, and Prakash V. A. K. Ramdass. "Lupus Erythematosus Tumidus Misdiagnosed as Erythema Nodosum from Coccidioidomycosis." Case Reports in Dermatology 16, no. 1 (2024): 128–32. http://dx.doi.org/10.1159/000538737.

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Introduction: Lupus erythematosus tumidus (LET) is a rare photosensitive dermatosis that is categorized as intermittent cutaneous lupus erythematosus. It shares clinical similarities and histopathological features with other skin disorders, such as erythema nodosum, lymphocytic infiltrate of Jessner, and reticular erythematous mucinosis, thus making diagnosis quite challenging. We present a patient with LET whose diagnosis was confirmed after seeing several doctors. Case Presentation: A 52-year-old Hispanic female presented with tender erythematous nodules on her thighs for approximately 1 mon

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8

Kim, Esther K., Peter W. Hashim, and Saakshi Khattri. "Subacute Cutaneous Lupus Erythematosus Coexisting in a Patient with Plaque Psoriasis." Journal of Psoriasis and Psoriatic Arthritis 2, no. 2 (2017): 62–64. http://dx.doi.org/10.1177/247553031700200204.

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Subacute cutaneous lupus erythematosus (SCLE) is a form of cutaneous lupus erythematosus that is characterized by nonscarring, erythematous, annular eruptions occurring mainly on sun-exposed areas. The incomplete understanding of SCLE creates challenges in diagnosis and treatment. This report describes the rare case of SCLE co-existing with plaque psoriasis.

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9

Parimala L and Vanitha R. "Assess the knowledge regarding the risk of cardiovascular diseases among systemic lupus erythematosus patient." International Journal of Research in Pharmaceutical Sciences 10, no. 4 (2019): 2739–41. http://dx.doi.org/10.26452/ijrps.v10i4.1539.

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India is a country with different beliefs like religious, cultural, variation and economic diversity in the health care setting. SLE is a long term disease which involves multisystem, leading to loss of immune tolerance to own antigens. The study aims to assess the knowledge regarding the risk of cardiovascular diseases among systemic lupus erythematous patient at Saveetha Medical College and Hospital. A quantitative research approach was adopted with convenient sampling technique to select 60 patients with systemic lupus erythematosus who attend at Saveetha Medical College and Hospital. Data

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Bernard, Heather, and Corinna Rea. "Neonatal lupus presenting as a non-specific rash in primary care." BMJ Case Reports 13, no. 12 (2020): e237463. http://dx.doi.org/10.1136/bcr-2020-237463.

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Neonatal lupus erythematosus is a rare autoimmune disease caused by passive transplacental acquisition of maternal autoantibodies manifesting in cutaneous, cardiac, haematological and hepatobiliary abnormalities. The hallmark dermatological finding is erythematous annular lesions with a predilection for photo-exposed areas of the skin. We present a case of a female infant born to a mother with Sjogren’s syndrome, who initially presented to an ambulatory care setting with non-specific erythematous papules involving the face and scalp. Within 6 days the rash changed in appearance, consisting of

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Baharudin, Ruziana, Nur Suhaila Idris, Juliawati Muhammad, and Wan Noor Hasbee Wan Abdullah. "A Case Report of Male Systemic Lupus Erythematous with Antinuclear Antibodies-Negative: A Challenging Diagnosis." Korean Journal of Family Medicine 43, no. 2 (2022): 150–54. http://dx.doi.org/10.4082/kjfm.20.0211.

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Systemic lupus erythematosus (SLE) is a connective tissue disease of unknown etiology that predominantly affects women of childbearing age. We report a case of male systemic lupus erythematous with antinuclear antibodies and typical clinical presentations of multiple skin lesions, polyarticular joint pain, fatigue, anorexia, and hair loss. Full evaluations were used to establish a diagnosis of SLE. The lower prevalence of SLE among males and antinuclear antibody-negative patients poses a great challenge for diagnosis. Therefore, as primary care doctors, we need to have a high suspicion of syst

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Subiantoro, Risza. "MANAGEMENT OF DEPRESSION IN CHILDREN WITH LUPUS ERYTHEMATOSUS SYSTEM." Jurnal Psikiatri Surabaya 10, no. 2 (2021): 74. http://dx.doi.org/10.20473/jps.v10i2.23659.

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CASE REPORTMANAGEMENT OF DEPRESSION IN CHILDREN WITH LUPUS ERYTHEMATOSUS SYSTEMRisza Subiantoro*, Nining Febriyana**, Lestari Basoeki**, Endang Wasiki** *Participant in Specialist I Psychiatric / Psychiatric Education Program, Faculty of Medicine, Universitas Airlangga / Dr. Soetomo General Hospital, Surabaya, Indonesia Bumi Panua Hospital, Pohuwato, Gorontalo, Indonesia** Psychiatrist (Consultant), Teaching Staff at Department / SMF Psychiatry, Faculty of Medicine, Universitas Airlangga / Dr. Soetomo General Hospital, Surabaya, Indonesia ABSTRACT Depression is a comorbid in patients with Syst

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13

Bullock, Taylor, Robert Simonds, Jeffrey McBride, Mawish Irfan, and Sarah Young. "Neonatal Lupus Erythematosus: A Case Report and Review of the Literature." SKIN The Journal of Cutaneous Medicine 7, no. 2 (2023): 649–56. http://dx.doi.org/10.25251/skin.7.2.1.

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Neonatal lupus erythematosus (NLE) is a rare autoimmune condition caused by transplacental passage of maternal IgG autoantibodies to the fetus. It often presents with erythematous annular lesions on the scalp and periorbital area that appear after exposure to sunlight. Clinicians should be aware of the broad manifestations of neonatal lupus erythematosus, including cutaneous, cardiac, hematologic, hepatic and neurological manifestations. We present a case of cutaneous neonatal lupus erythematosus with rare central nervous system findings and perform a literature review on the subject.

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14

Frey, Marcos Noronha, Ana Elisa Empinotti Ioppi, Gabriela Czarnobay Garbin, Roque Domingos Furian, and Ana Elisa Kiszewski Bau. "Congenital and neonatal lupus erythematosus: two case reports." Anais Brasileiros de Dermatologia 87, no. 4 (2012): 625–28. http://dx.doi.org/10.1590/s0365-05962012000400019.

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Neonatal lupus erythematosus is an autoimmune disease produced by the passage of maternal antinuclear antibodies and extractable nuclear antigen antibodies through the placenta. At the moment of the diagnosis, the mothers are asymptomatic in 40 to 60% of cases. The most common manifestations are cutaneous lesions and congenital heart block. The cutaneous findings are variable and usually begin within the first weeks or months of life. Congenital lupus erythematosus is a congenital variant of neonatal lupus erythematosus. We present one case of congenital lupus erythematosus and one case of neo

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15

Santiago, Luís, Rosa Mascarenhas, Óscar Tellechea, and Margarida Gonçalo. "Toxic epidermal necrolysis-like subacute cutaneous lupus erythematosus associated with lung carcinoma." BMJ Case Reports 12, no. 10 (2019): e231152. http://dx.doi.org/10.1136/bcr-2019-231152.

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Specific vesiculobullous skin lesions in lupus erythematosus (LE) are rare and must be differentiated from toxic epidermal necrolysis (TEN), TEN-like dermatoses and other vesiculobullous conditions. We report a patient with typical subacute cutaneous lupus erythematous that progressed with large sheet-like areas of epidermal detachment and Nikolsky sign resembling TEN. She had a serological profile suggestive of underlying connective tissue disease, histological findings of interface dermatitis with a lymphocytic infiltrate, positive direct immunofluorescence, resolution with immunomodulation

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16

Singh, Sukhraj, Sandra Sheffield, Nisha Chowdhury, Swetha Nuthulaganti, Zareen Vaghaiwalla, and Karishma Ramsubeik. "Utilization of Rituximab for Refractory Rowell Syndrome." Case Reports in Rheumatology 2021 (July 29, 2021): 1–6. http://dx.doi.org/10.1155/2021/2727382.

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Rowell syndrome describes the occurrence of erythema multiforme-like lesions in patients with cutaneous lesions of lupus erythematosus. The clinical picture of atypical erythema multiforme-like lesions, presence of chilblains, speckled ANA pattern, anti-Ro/SSA, or anti-La/SSB antibodies, and absence of infectious or pharmacologic triggers in a patient with systemic lupus erythematosus are some of the classic clinical and serologic features. Histopathologic and serologic findings can help differentiate this process from erythema multiforme. We present a case of young woman with systemic lupus e

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Karasińska, Aneta, Adriana Polańska, Monika Bowszyc‑Dmochowska, Ryszard Żaba, Zygmunt Adamski, and Aleksandra Dańczak‑Pazdrowska. "Discoid lupus erythematosus – a case report, diagnostic and therapeutic difficulties." Journal of Face Aesthetics 4, no. 2 (2021): 135–44. http://dx.doi.org/10.20883/jofa.51.

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Discoid lupus erythematosus is the most common clinical manifestation of lupus erythematosus. Characteristic features are erythematous plaques with follicular hiperkeratosis, clearly demarcated from surrounding skin, that resolve with atrophy and scarring, leading to significant aesthetic defects. The consequence of involving the scalp is cicatrical alopecia. On the ground of long lasting, untreated lesions squamous cell carcinoma (SCC) may develop. On the other hand SCC remains in the circle of DLE differentiation. We present diagnostic and therapeutic difficulties associated with DLE.

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18

Mrabat, Samia, Hanane aybay, Zakia Douhi, Sara Elloudi, Fatima Zahra Mernissi, and Mouna Rimani. "Cutaneous lupus tumidus: An unusual unilateral presentation." Our Dermatology Online 12, no. 2 (2021): 151–52. http://dx.doi.org/10.7241/ourd.20212.10.

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Lupus tumidus is a rare subtype of chronic cutaneous lupus erythematosus characterized by erythema and bright urticarial erythematous and violaceous lesions on sun-exposed areas that heal without leaving scars. Lupus tumidus follows a benign and intermittent clinical course and is rarely associated with systemic lupus erythematosus. Treatment involves photoprotection, topical corticosteroids, and antimalarials. We report the case of a 42-year-old patient with an atypical unilateral form of lupus tumidus successfully treated with the administration of hydroxychloroquine in combination with phot

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19

Richter, JG, O. Sander, M. Schneider, and P. Klein-Weigel. "Diagnostic algorithm for Raynaud’s phenomenon and vascular skin lesions in systemic lupus erythematosus." Lupus 19, no. 9 (2010): 1087–95. http://dx.doi.org/10.1177/0961203310374304.

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Skin discolorations and skin lesions due to vascular pathologies are common clinical features in systemic lupus erythematosus. A variety of clinical manifestations such as Raynaud’s phenomenon, acrocyanosis, livedo patterns, erythematous or violaceous macules and papules or necrosis are triggered by heterogeneous pathophysiological mechanisms such as vasospasm, vasculitis or thromboembolism. A standardized macro- and microvascular assessment is necessary to establish the correct diagnosis. We describe and illustrate common clinical features of vascular skin manifestations in systemic lupus ery

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Nakamura, Satoshi, Tomoko Yamada, Naoka Umemoto, et al. "Cheek and Periorbital Peculiar Discoid Lupus Erythematosus: Rare Clinical Presentation Mimicking Tinea Faciei, Cutaneous Granulomatous Disease or Blepharitis." Case Reports in Dermatology 7, no. 1 (2015): 56–60. http://dx.doi.org/10.1159/000381208.

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We present clinically peculiar facial discoid lupus erythematosus (DLE) that mimicked tinea faciei. Although DLE is a chronic autoimmune dermatosis, it has a variety of rare clinical presentations, including periorbital DLE, comedonic DLE and hypertrophic DLE recently. In this case, a scaly, erythematous lesion on the eyelid and the central healed, mildly elevated, annularly distributed facial DLE mimicked tinea faciei, complicating our diagnosis.

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Wang, Chrong-Reen, and Cheng-Han Lee. "Pelvic deep venous thrombosis mimicking lower limb cellulitis in systemic lupus erythematosus-associated antiphospholipid syndrome." Lupus 31, no. 5 (2022): 613–18. http://dx.doi.org/10.1177/09612033221084230.

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Objectives Systemic lupus erythematosus (SLE) associated with antiphospholipid syndrome (APS) is a complex clinical scenario with thromboembolic events, lupus activity, and related therapeutic complications like infection. In SLE, iliofemoral (IF) deep vein thrombosis (DVT) with fever and erythematous swollen limbs mimic cellulitis over lower extremities. Nevertheless, to distinguish DVT from cellulitis is imperative in clinical practice due to the use of different therapeutic regimens. Methods A retrospective study was performed to analyze iliofemoral DVT in hospitalized SLE-associated APS pa

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Dijkmans, BA, W. Bergman, F. Eulderink, and KA Meijers. "Reticular erythematous mucinosis syndrome in a patient with polyarthritis." Acta Dermato-Venereologica 66, no. 5 (1986): 442–45. http://dx.doi.org/10.2340/0001555566442445.

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A patient with seronegative oligoarthritis who developed the reticular erythematous mucinosis (REM) syndrome is described. This syndrome is considered to be a dermatological entity unrelated to systemic disorders. Aggravation of the rash by exposure to sunlight and a good response to anti-malarial agents suggest a relationship with rheumatological disorders, e.g. rheumatoid arthritis and systemic lupus erythematosus. Dermatologists consulted by a patient with the REM syndrome should be aware of the possibility of an associated rheumatological disease.

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Kenny, Bret, Duane Lichtenwald, Glenda R. Wright, and Allison Osmond. "A case report of a localized reticular erythematous mucinosis like eruption of the lower legs mimicking cutaneous larvae migrans." SAGE Open Medical Case Reports 9 (January 2021): 2050313X2110030. http://dx.doi.org/10.1177/2050313x211003075.

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Reticular erythematous mucinosis is an uncommon type of cutaneous mucinosis. Typically, reticular erythematous mucinosis affects middle-aged women and usually appears as papules and plaques on the mid-upper trunk. Histologically, biopsies of reticular erythematous mucinosis reveal increased deposition of dermal mucin and perivascular lymphocytic inflammation. Infrequently, reticular erythematous mucinosis has been reported in males and in atypical locations other than the trunk. In these instances, reticular erythematous mucinosis can present a diagnostic challenge clinically and histologicall

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Huzairi Sani, Nada Syazana, and Malek Faris Riza Feisal. "A different kind of skin presentation in Systemic Lupus Erythematosus (SLE): A case report." Asian Journal of Medicine and Biomedicine 4, no. 1 (2020): 42–46. http://dx.doi.org/10.37231/ajmb.2020.4.1.329.

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Erythema nodosum is a septal panniculitis which is a variant of chronic cutaneous lupus erythematosus (CCLE). It is further classified in the group of Lupus Erythematous Panniculitis (LEP).[1] The most frequent cutaneous manifestations include indurated plaques, subcutaneous nodules and sometimes ulcerations. The lesions occur predominantly on the face, upper arms, upper trunk, breasts, buttocks and thighs.[2] They occur most frequently in adult females and do not typically manifest cutaneously in Systemic Lupus Erythematosus (SLE).[3] In this case report, we discuss a young gentleman who pres

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Anjani, I. Gusti Agung Dwi Putri, I. Wayan Eka Saputra, and Putu Dyah Widyaningsih. "Systemic lupus erythematous in men with interstitial lung pneumonia: a rare case report." International Journal of Advances in Medicine 11, no. 4 (2024): 384–88. http://dx.doi.org/10.18203/2349-3933.ijam20241633.

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Systemic lupus erythematosus (SLE) is a chronic autoimmune inflammatory disease with unknown etiology and very diverse clinical manifestations, disease course, and prognosis. It is most common in African-American women, the prevalence being 4 per 1000 females. SLE predominantly affects young women, most presenting between 20 and 40 years of age. Male SLE is rare, with only one male patient reported per nine females. Pulmonary involvement in SLE is various. SLE-associated interstitial lung disease (ILD), while rare, is a predictor of poor prognosis. We report a 50-year-old male patient with com

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Bakshi, Satvinder Singh. "Erythematous Candidiasis." Journal of Allergy and Clinical Immunology: In Practice 6, no. 2 (2018): 646. http://dx.doi.org/10.1016/j.jaip.2017.08.012.

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Aiempanakit, K., K. Chiratikarnwong, S. Juthong, and S. Auepemkiate. "Toxic epidermal necrolysis-like acute cutaneous lupus erythematosus in a patient with progressive systemic sclerosis." Lupus 27, no. 11 (2018): 1860–63. http://dx.doi.org/10.1177/0961203318789766.

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A 60-year-old female was diagnosed with progressive systemic sclerosis and interstitial lung disease of two months’ duration. The patient was treated for Raynaud phenomenon with aspirin, nifedipine, colchicine, and naproxen. Two weeks after treatment, she developed widespread erythematous patches with blistering eruptions on the face, torso, and extremities, and also had erosion on the oral mucosa. Skin biopsy for histopathology and direct immunofluorescent studies were suggestive of lupus erythematosus. To the best of our knowledge, this is the first case of toxic epidermal necrolysis-like ac

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Chikhalkar, Siddhi Bhalchandra, Surender Singh, Avani Jatin Kumar Shah, Bhushan Madke, and Yallappa Ramchandrappa Kabbannavar. "Halting the Progression of Cicatricial Alopecia with Injectable Platelet-Rich Fibrin." International Journal of Trichology 15, no. 4 (2023): 163–66. http://dx.doi.org/10.4103/ijt.ijt_116_21.

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Discoid lupus erythematosus (DLE) is a chronic variant of cutaneous lupus erythematosus characterized by well-defined erythematous plaques with adherent scales and follicular plugging. The affected scalp shows erythema, edema, atrophy, alopecia, and telangiectasia. Trichoscopy of DLE shows branching capillaries, white patches, keratin plugs, reduced follicular ostia, and white dots and blue-gray dots arranged in speckles pattern. Prompt diagnosis and aggressive, early multimodal therapy helps in preventing disfiguring hair loss and psychosocial sequelae. Hereby, we present a case of reversal o

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Oh, Il Hwan, Kyoung Hoon Rhee, and One Zoong Kim. "Prediction of <i>Helicobacter pylori</i> Infection by Endoscopic Severity of Erythematous Gastritis in Asymptomatic Adults." Korean Journal of Medicine 98, no. 4 (2023): 191–98. http://dx.doi.org/10.3904/kjm.2023.98.4.191.

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Background/Aims: <i>Helicobacter pylori</i> (<i>H. pylori</i>) infection is correlated with erythematous gastritis, which is one of the endoscopic findings of the Sydney classification system. The present study evaluated the association between the endoscopic severity of erythematous gastritis and <i>H. pylori</i> infection.Methods: We prospectively enrolled asymptomatic adults who were diagnosed with erythematous gastritis during screening esophagogastroduodenoscopy. A rapid urease test was performed in all participants to diagnose <i>H. pylori</i&

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Gao, Lin, Jane Liesveld, Jennifer Anolik, Andrew Mcdavid та Richard John Looney. "IFNβ signaling inhibits osteogenesis in human SLE bone marrow". Lupus 29, № 9 (2020): 1040–49. http://dx.doi.org/10.1177/0961203320930088.

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Background Bone marrow mesenchymal stem cells are multipotent adult stem cells that can differentiate into osteoblasts, adipocytes, and chondrocytes. Our recently published data demonstrate that systemic lupus erythematous bone marrow mesenchymal stem cells produce increased quantities of interferon β based on a positive feedback loop involving the innate signaling molecule mitochondrial antiviral signaling protein. Moreover, this pathway contributes to human systemic lupus erythematous bone marrow mesenchymal stem cell senescence-like features. Here we investigate the differentiation defects

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SATO, Seisho, Yoko FUYUNO, Shotaro KAWANO, and Masutaka FURUE. "A Case of Reticular Erythematous Mucinosis with Systemic Lupus Erythematosus." Nishi Nihon Hifuka 82, no. 6 (2020): 401–2. http://dx.doi.org/10.2336/nishinihonhifu.82.401.

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Ocon, Anthony, Eduardo Avalos Sugastti, and Nananamibia Duffy. "Impressive resolution of refractory hypertrophic discoid lupus erythematosus with anifrolumab." BMJ Case Reports 17, no. 6 (2024): e258487. http://dx.doi.org/10.1136/bcr-2023-258487.

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Hypertrophic discoid lupus erythematosus is a rare variant of chronic cutaneous lupus erythematosus and is often challenging to treat. A male in his early 60s presented with diffuse erythematous, crusty, pruritic plaques on his upper and lower extremities, face, upper back, dorsal aspect of the hands and chest. He also described prolonged morning stiffness, swelling of his fingers and wrists, oral sores and Raynaud’s phenomenon. He was positive for antinuclear antibody and anti-SSA antibody and had low C3 and C4 proteins. The skin biopsy was consistent with hypertrophic discoid lupus erythemat

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Takezawa, K., I. Ueda-Hayakawa, F. Yamazaki, N. Kambe, Y. Son, and H. Okamoto. "Successful treatment with hydroxychloroquine for systemic lupus erythematosus with cutaneous involvement accompanied by a xanthomatous reaction." Lupus 29, no. 1 (2019): 79–82. http://dx.doi.org/10.1177/0961203319890677.

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Antimalarials are usually recommended for the first-line systemic treatment of cutaneous lupus erythematosus. Alopecia in patients with discoid lupus erythematosus (DLE) is sometimes a refractory condition in spite of topical therapies. We herein described a case of DLE on the scalp with a pathological change of a xanthomatous reaction, which was successfully treated with hydroxychloroquine (HCQ). A 34-year-old woman presented with hair loss to the parietal region. She had been diagnosed with systemic lupus erythematosus (SLE) four years previously. Treatment with 30 mg/day of prednisolone (PS

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Le, Marilyn, Payvand Kamrani, and L. Claire Hollins. "Coexistentence of Morphea and DLE in a Patient with Beta Thalassemia Leading to a Diagnosis of Systemic Lupus Erythematous." SKIN The Journal of Cutaneous Medicine 6, no. 3 (2022): 243–45. http://dx.doi.org/10.25251/skin.6.3.11.

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Patients with autoimmune disorders are predisposed to developing a second autoimmune condition. This can be applied to cutaneous conditions as well. Morphea or localized scleroderma is an autoimmune inflammatory and fibrosing skin disorder due to increased collagen deposition.1,2 Patients with morphea are four times likelier of having a concomitant autoimmune disease.1 There have been cases of systemic lupus erythematosus (SLE) with morphea, but the co-occurrence of discoid lupus erythematosus (DLE) with morphea has been rarely reported, and never reported in patient with Beta-thalamessmia.1,2

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Vaishnavi, Kanajam Swetha Sri, Aswanth KS, and Thirunavukkarasu Arun Babu. "Juvenile recurrent parotitis." BMJ Case Reports 17, no. 12 (2024): e262596. https://doi.org/10.1136/bcr-2024-262596.

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A child in middle childhood presented with six episodes of left-sided parotitis in the last 6 months. This was associated with erythematous circinate patches of the dorsal aspect of the tongue suggestive of geographic tongue. His growth was normal with no underlying nutritional deficiencies. Relevant investigations ruled out immune conditions like Sjogren’s syndrome, lupus erythematosus and immunodeficiencies. The child had a complete resolution on conservative management. This case depicts a rare association of two uncommon entities.

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Ha, Dae-Lyong, Gi-Wook Lee, Kihyuk Shin, et al. "Unilateral facial erythematous patch as the presenting sign of systemic lupus erythematosus." Lupus 29, no. 14 (2020): 1968–70. http://dx.doi.org/10.1177/0961203320957739.

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Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder that can have many cutaneous manifestations including malar rash, discoid rash or oral ulcer. Isolated unilateral involvement of face is uncommon in SLE. It lacks typical clinical features of LE, and may impose a diagnostic challenge for clinicians. Herein we report a case of 62-year-old woman presenting with a 2-year history of erythematous patches on left cheek and eyelid. Initially, she was diagnosed as having recurrent blepharitis or cellulitis that did not respond to conventional treatment with ophthalmic medicaments. As

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Alharbi, Samar, and Jorge Sanchez-Guerrero. "Successful Treatment of Urticarial Vasculitis in a Patient With Systemic Lupus Erythematosus With Rituximab." Clinical Medicine Insights: Arthritis and Musculoskeletal Disorders 13 (January 2020): 117954412096737. http://dx.doi.org/10.1177/1179544120967374.

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Urticarial vasculitis is an eruption of erythematous wheals that clinically resemble urticaria but histologically show changes of leukocytoklastic vasculitis. In association with connective tissue disease it is most commonly seen complicating Systemic lupus erythematous (SLE) and, less often, Sjogren’s syndrome. Here, we report a 25-year-old woman who developed SLE in 1998. In May 2013 she presented with urticarial vasculitis; her skin biopsy was consistent with leukocytoclastic vasculitis. She also developed bilateral uveitis. She had most of the clinical and laboratory characteristics of hyp

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Earlia, Nanda, Zulfan Zulfan, Aldilla Pradistha, et al. "Coexistence of Psoriasis Vulgaris and Systemic Lupus Erythematosus: A Rare Clinical Case." Indonesian Journal of Case Reports 3, no. 1 (2025): 11–15. https://doi.org/10.60084/ijcr.v3i1.278.

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Psoriasis vulgaris is a chronic skin inflammation characterized by the appearance of clearly limited erythematous plaques, along with rough, thick, and silvery-white scales. Systemic Lupus Erythematosus (SLE) is a multifactorial autoimmune disease with diverse clinical manifestations and can involve one or more organs. This case report presents a patient with Psoriasis Vulgaris with SLE. A 47-year-old woman presented with erythematous plaque lesions with thick scales and some hyperpigmentation, numerous, plaque-sized lesions with regional distribution on the scalp, right and left cubital areas

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Chekhovska, G. S. "ROLE OF DERMATOSCOPY IN CHRONIC DERMATOSES DIAGNOSIS." International Medical Journal, no. 2 (July 15, 2020): 53–56. http://dx.doi.org/10.37436/2308-5274-2020-2-11.

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Dermatoscopy is a valuable auxiliary non−invasive method used in the diagnosis of inflammatory, parasitic and viral skin diseases. Treatment of dermatoses is based on the results of analysis of melanin, follicular−horny and vascular components. Diagnosis begins with polarized dermatoscopy and then progresses to non−polarized using immersion fluid. At dermatoscopic inspection of a psoriatic plaque the point vessels evenly distributed along all the surface (a symptom of "scattered red pepper") are noted. Eczema is characterized by focal accumulation of blood vessels in the form of dots, peeling,

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Police, Rani* Gowri Sunanda Shaik Ali Basha. "SYSTEMIC LUPUS ERYTHEMATOUS IN A MALE PATIENT – A RARE INCIDENCE." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 01 (2018): 547–51. https://doi.org/10.5281/zenodo.1162752.

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Systemic lupus erythematosus (SLE) is an auto immune connective tissue disease in which the body immune system mistakenly attacks healthy tissue in many parts of the body, where vascular lesions are one of the typical symptoms. The pathological progress often involves skin vessels, renal glomeruli, cardiovascular system, brain, lung alveoli, and gastrointestinal tract vessels. We report a case of 35 year, old male patient who admitted in our hospital with rashes, fever, vomiting, severe joint pains, hair loss and burning sensation in stomach and was diagnosed to have SLE by anti nuclear antibo

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Pozo, J. Del, C. Peña, M. Almagro, M. T. Yebra, and W. Martínez. "Systemic lupus erythematosus presenting with a reticular erythematous mucinosis-like condition." Lupus 9, no. 2 (2000): 144–46. http://dx.doi.org/10.1191/096120300678828028.

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Rekik, Mariem, Khadija Sellami, Massara Baklouti, Emna Bahloul, and Hamida Turki. "Oral involvement in lupus erythematosus: A report of three cases." Our Dermatology Online 13, no. 4 (2022): 467–68. http://dx.doi.org/10.7241/ourd.20224.31.

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Sir, Lupus erythematosus (LE) is an autoimmune disease that may rarely affect the oral mucosa. This mucosal damage may be mistaken for lichen planus. Herein, we report three cases of oral lupus. Observation 1: A 41-year-old female, with a seven-year history of systemic LE (SLE) treated with hydroxychloroquine, presented for recent food discomfort. An examination of the oral mucosa found an erythematous plaque on the palate (Fig. 1) and whitish macules on the cheek mucosa. A palatal biopsy was in favor of lupus.

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Hlavatá, Marcela. "Reticular erythematous mucinosis." Dermatologie pro praxi 14, no. 3 (2020): 155–56. http://dx.doi.org/10.36290/der.2020.029.

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Graves, Julia E., and Robert T. Brodell. "Erythematous scaling eyelids." Postgraduate Medicine 117, no. 6 (2005): 43–45. http://dx.doi.org/10.3810/pgm.2005.06.1664.

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Riyaz, Najeeba, and A. Riyaz. "Erythematous polycyclic patches." Indian Journal of Dermatology, Venereology and Leprology 72, no. 5 (2006): 398. http://dx.doi.org/10.4103/0378-6323.27773.

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Griffin, JohnR, OlgaV Udovenko, and DirkM Elston. "Asymptomatic erythematous plaque." Indian Dermatology Online Journal 6, no. 6 (2015): 419. http://dx.doi.org/10.4103/2229-5178.169721.

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Lotti, T., M. Benci, and B. Lorusso. "Reticular erythematous mucinosis." Journal of the European Academy of Dermatology and Venereology 3, no. 1 (1994): 63–66. http://dx.doi.org/10.1111/j.1468-3083.1994.tb00073.x.

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Ridley, C. M. "Lupus erythematous profundus." Clinical and Experimental Dermatology 14, no. 4 (1989): 333. http://dx.doi.org/10.1111/j.1365-2230.1989.tb02002.x.

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de Oliveira Rocha, Bruno, Tarsila Carvalho dos Santos, and Juliana Dumêt Fernandes. "Erythematous swollen ears." JDDG: Journal der Deutschen Dermatologischen Gesellschaft 12, no. 3 (2014): 269–71. http://dx.doi.org/10.1111/ddg.12223.

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Isaacson, Glenn. "The erythematous eardrum." Visual Journal of Emergency Medicine 21 (October 2020): 100887. http://dx.doi.org/10.1016/j.visj.2020.100887.

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