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Journal articles on the topic 'Pemfigoid'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Istiqomah, Annisah, and Wizar Putri Mellaratna. "Seorang Laki-Laki Usia 68 tahun dengan Pemfigoid Bulosa." GALENICAL : Jurnal Kedokteran dan Kesehatan Mahasiswa Malikussaleh 2, no. 1 (2023): 66. http://dx.doi.org/10.29103/jkkmm.v2i1.9311.

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Pemfigoid bulosa adalah penyakit autoimun kronik yang ditandai dengan lepuh subepiderrnal berdinding tegang. Pemfigoid bulosa paling sering terjadi pada usia tua terutama di atas 60 tahun dengan puncak kejadian di atas usia 70 tahun, kasus pada anak jarang terjadi. Frekuensi pada laki-laki sama dengan perempuan. Etiologi pemfigoid bulosa adalah autoimun, tetapi penyebab yang menginduksi produksi autoantibodi pada sampai saat ini masih belum jelas. Pemfigoid bulosa dipicu oleh sinar Ultraviolet (UV), baik UVB dan Ultraviolet A Light (PUVA), dan terapi radiasi.

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2

Janiszewska, Kamila, Małgorzata Kurpios-Kosińska, and Bogusława Rudnicka. "Pemfigoid ciężarnych – studium przypadku." Pielęgniarstwo Polskie 90, no. 4 (2023): 141–45. http://dx.doi.org/10.20883/pielpol.2023.12.

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3

Günaydın, Aslı, Bengü Gerçeker Türk, Gülşen Kandiloğlu, and Tuğrul Dereli. "Vulvar Sikatrisyel Pemfigoid: Bir Çocuk Olgu." TURKDERM 48, no. 1 (2014): 51–53. http://dx.doi.org/10.4274/turkderm.92603.

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4

Komilov, Haydar Pazilovich, Malika Xudayberganova Ibragimova, Dilnoza Anvarovna Abduvaxobova, and Zilola Xaydarovna Adilxo'jaeva. "OG'IZ BO'SHLIG'I SHILLIQ QAVATI QIZIL YASSI TEMIRATKISINING TURLI SHAKLLARINI KLINIK KO'RINISHINING XUSUSIYATLARI." Multidisciplinary Journal of Science and Technology 5, no. 5 (2025): 1215–23. https://doi.org/10.5281/zenodo.15532058.

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Ushbu tadqiqotning asosiy maqsadi – ogʻiz boʻshligʻi shilliq qavatida uchraydigan qizil yassi temiratkining giperkeratotik (oddiy), eroziv, yarali, pemfigoid va soʻgalsimon shakllari bilan kechadigan klinik holatini chuqur oʻrganishdan iborat.

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5

Sihombing, Rasco Sandy, Henry Ratno Diono Silalahi, Hamzah Shatri, et al. "Diagnosis dan Tata Laksana Acquired Hemophilia A (AHA) dengan Pemfigoid Bulosa." Jurnal Penyakit Dalam Indonesia 3, no. 4 (2017): 218. http://dx.doi.org/10.7454/jpdi.v3i4.56.

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Acquired hemophilia A merupakan kondisi dimana faktor koagulasi VIII menjadi tidak aktif akibat pembentukan autoantibodi. Kondisi ini dikaitkan dengan kehamilan, keganasan, dan penyakit auitoimun dengan kelainan kulit. Pada kasus ini, seorang wanita berusia 66 tahun, datang dengan keluhan perdarahan paska tindakan yang disertai dengan lesi kulit. Pasien didiagnosis dengan acquired hemophilia A dengan ditemukannya inhibitor faktor VIII terkait dengan pemfigoid bulosa.Kata Kunci: Acquired hemophilia A, diagnosis, pemfigoid bulosa, tata laksana Diagnosis and Treatment of Acquired Hemophilia A (AH

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6

SANTOS, JúLLIAN KAREN BEZERRA DOS, RODRIGO DAS NEVES SILVA, SHIRLENE SANTANA SANTOS NOBRE, et al. "ORAL BENIGN PEMFIGOID OF MUCOUS MEMBRANES: CASE REPORT." Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 130, no. 3 (2020): e215. http://dx.doi.org/10.1016/j.oooo.2020.04.498.

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7

Rudneva, N. S., T. G. Sadunashvili, Ya Yu Chumakova, E. V. Natarova, and A. V. Losev. "Case of bullous pemphigoid in patient with psoriasis, after new coronavirus infection COVID‑19." Medical alphabet, no. 27 (November 2, 2021): 48–51. http://dx.doi.org/10.33667/2078-5631-2021-27-48-51.

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In this work we discuss a case of Bullosus pemfigoid (B.P.) developed after pneumonia caused by new coronavirus disease COVID‑19 in a patient with psoriasis. Provided description is supported with the data of histological and serologic analysis, the lgG of epithelial basement membrane was detected to antigen ВР230-CF and to antigen ВР180-NC16A.

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8

Grzeszczuk, Mariola, Anna Woźniacka, Agnieszka Żebrowska, and Martyna Skręta-Śliwińska. "Pemphigoid nodularis – diagnostic challenges." Dermatology Review 109, no. 4 (2022): 291–98. http://dx.doi.org/10.5114/dr.2022.123984.

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9

Trisnowati, Dwi M., Hyacintha P. Budi, Shienty Gaspersz, and Meilany Durry. "Bullous Pemphigoid Treated with Corticosteroid: A Case Report." e-CliniC 10, no. 2 (2022): 400. http://dx.doi.org/10.35790/ecl.v10i2.41403.

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Abstract: Bullous pemphigoid (BP) is an autoimmune disease clinically characterized by pruritic, large, tense subepidermal bullae over normal skin, erythematous or urticarial plaques. The pathogenesis related to the immune system towards BP antigen 180 and 230. Mild lesions may be treated with topical corticosteroid but the more extensive lesions are treated with oral corticosteroids. We reported a case of 58-year-old man came with clear fluid-filled blisters on the body since a week ago. Dermatological examination revealed multiple vesicle-bullae, filled with clear fluid, tense walls. Nikolsk

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10

ÇANKAYA, Cem, and Yakup YILDIZLI. "Ocular Cicatricial Pemphigoid Activation After COVID-19 Infection." Turkiye Klinikleri Journal of Ophthalmology 31, no. 3 (2022): 187–90. http://dx.doi.org/10.5336/ophthal.2021-85100.

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11

Woźniak, Katarzyna, Marian Dmochowski, Waldemar Placek, et al. "Pemphigoid – diagnosis and treatment. Polish Dermatological Society Consensus." Dermatology Review 1 (2016): 19–34. http://dx.doi.org/10.5114/dr.2016.57738.

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12

Skutil, Marcin M., and Ryszard Roztoczyński. "Pemphigoid gestationis – a rare dermatosis of the prenatal period. Case report." Dermatology Review 3 (2016): 209–13. http://dx.doi.org/10.5114/dr.2016.60624.

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13

Dominiak, Małgorzata P., Sebastian K. Kłosek, Zofia Gerlicz-Kowalczuk, Joanna Krzysiek, Aleksandra Kobusiewicz, and Andrzej Kaszuba. "Bullous pemphigoid resembling erythema gyratum repens – case report." Dermatology Review 4 (2017): 439–45. http://dx.doi.org/10.5114/dr.2017.69769.

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14

Kalińska-Bienias, Agnieszka, Anna Leśniewska, Piotr Bienias, Cezary Kowalewski, and Katarzyna Woźniak. "Psoriasis vulgaris, bullous pemphigoid, metabolic syndrome – coincidence or common pathogenetic background?" Dermatology Review 4 (2014): 294–98. http://dx.doi.org/10.5114/dr.2014.45123.

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15

Wieczorek, Aleksandra, Jacek Szepietowski, Katarzyna Łoza, et al. "Bed bug bites mimicking bullous pemphigoid: a report of two cases." Dermatology Review 4 (2016): 281–84. http://dx.doi.org/10.5114/dr.2016.61775.

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16

Kručaitė, Augustė, and Alina Vilkaitė-Kitkovskė. "Specifinės nėščiųjų dermatozės." Lithuanian General Practitioner 28, no. 6 (2024): 468–75. http://dx.doi.org/10.37499/lbpg.1452.

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Tyrimo tikslas. Apibūdinti nėščiųjų specifines dermatozes ir aprašyti jų patofiziologiją, kliniką, diagnostiką ir gydymą, remiantis naujausiais tyrimais ir moksline literatūra. Metodai. Straipsnių paieška atlikta naudojant tarptautinę duomenų bazę „PubMed“. Į tyrimą įtraukti straipsniai, per pastaruosius 5–10 m. publikuoti anglų kalba. Rezultatai. Nėščiųjų specifinės dermatozės apima polimorfinį nėščiųjų išbėrimą, atopinį nėščiųjų dermatitą, gestacinį pemfigoidą ir intrahepatinę nėščiųjų cholestazę. Šios dermatozės nėščiosioms sukelia nerimą, diskomforto jausmą, pasireiškus išbėrimams ir inten

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17

Taniowas, Paul O., Tara S. Kairupan, Marlyn G. Kapantow, and Aryani Adji. "Bullous Pemphigoid in a Women with Type 2 Diabetes Mellitus: A Case Report." e-CliniC 10, no. 1 (2022): 131. http://dx.doi.org/10.35790/ecl.v10i1.39085.

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Abstract: Bullous Pemphigoid (BP) is an autoimmune disease with subepidermal blisters that are generally minimally itchy to non-itchy. It usually occurs in old age, but sometimes in children and young adults. Clinical presentation shows large, tense-walled blisters on normal or erythematous skin, mostly at the folds, lower abdomen, thighs, but they can appear anywhere. Therapy of BP is aimed to treat skin and mucous lesions as soon as possible and to reduce itchiness, therefore, the quality of life will be improved. The first line therapy is oral and topical corticosteroids, with an initial do

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18

AŞİRAN SERDAR, Zehra, Ezgi AKTAŞ KARABAY, Şirin YAŞAR, and Nihan KAZAZ. "Clinical Features, Associated Systemic Diseases, Mortality Rates, and Treatment Protocols in a Group of Turkish Patients with Bullous Pemphigoid." Turkiye Klinikleri Journal of Dermatology 28, no. 2 (2018): 44–50. http://dx.doi.org/10.5336/dermato.2018-61536.

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19

Mellyanawati, Mellyanawati. "One Case Suspected Chronic Bullous Disease in Childhood." Jurnal Ilmiah Kedokteran Wijaya Kusuma 10, no. 2 (2021): 176. http://dx.doi.org/10.30742/jikw.v10i2.1364.

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Penyakit bula pada anak sangat beraneka ragam, mulai dari yang paling sering adalah impetigo bulosa dan epidermolysis bulosa. Sedangkan penyakit bulosa lain pada anak yang lebih jarang dijumpai adalah penyakit bulosa linear IgA pada anak, pemfigoid bulosa dan sistemik lupus eritematosus bulosa. Salah satu varian dari penyakit bulosa linear Ig A pada anak adalah Chronic bullous disease in childhood (CBDC) yaitu suatu penyakit autoimun yang jarang dijumpai dan muncul pada usia prepubertas. Ciri khas dari penyakit ini adalah timbulnya lepuh yang muncul secara mendadak dan biasanya lesi yang baru

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20

Carbone, M., P. L. Calogiuri, and R. Broccoletti. "Il pemfigoide delle membrane mucose." Italian Oral Surgery 9, no. 2 (2010): 89–92. http://dx.doi.org/10.1016/j.ios.2010.01.003.

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21

Asriye; PALA, MOCAN. "Mükoz membran pemfigoidi – bir olgu sunumu." Ankara Üniversitesi Diş Hekimliği Fakültesi Dergisi 37, no. 1 (2010): 45–50. http://dx.doi.org/10.1501/dishek_0000000113.

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22

Vaivadaitė, Urtė, Aistė Jankevičiūtė, and Karolis Pampikas. "GESTACINIO PEMFIGOIDO DIAGNOSTIKOS IR GYDYMO YPATUMAI." Health Sciences 33, no. 3 (2023): 190–92. http://dx.doi.org/10.35988/sm-hs.2023.116.

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Gestacinis pemfigoidas (GP) yra reta autoimuninė liga, priklausanti nėščiųjų dermatozių grupei. Klinikai būdingi uždegiminiai odos bėrimai: papulės, plokštelės, pūslelės ir pūslės bei jaučiamas stiprus niežulys. Tai viena rečiausių nėščiųjų dermatozių, tačiau negydant gali atsirasti nepalankių nėštumui ir vaisiui komplikacijų. Siekiant to išvengti, svarbi ankstyva diagnostika ir savalaikis ligos gydymas.

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23

Carbone, M., A. Gambino, and R. Broccoletti. "Il pemfigo." Italian Oral Surgery 11, no. 1 (2012): 37–40. http://dx.doi.org/10.1016/j.ios.2011.07.001.

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24

... "Bisoprolol ile İlişkili Liken Planus Pemfigoides." Turkderm 46, no. 2 (2012): 101–3. http://dx.doi.org/10.4274/turkderm.23540.

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25

Mergoni, Giovanni, Antonio Teoli, Roberto Ricci, Paolo Vescovi, and Maddalena Manfredi. "L’immunofluorescenza diretta nella diagnosi del pemfigoide delle membrane mucose: studio retrospettivo." Dental Cadmos 89, no. 01 (2021): 28. http://dx.doi.org/10.19256/d.cadmos.01.2021.06.

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26

Adomaitienė, Aida, Eglė Zinkevičienė, and Vesta Kučinskienė. "Nėščiųjų dermatozės." Lithuanian General Practitioner 24, no. 10 (2020): 708–11. http://dx.doi.org/10.37499/lbpg.603.

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Hormoniniai, imunologiniai ir fiziniai pokyčiai nėštumo laikotarpiu sukelia fiziologinius odos pokyčius, kurie vargina daugiau nei 90 proc. nėščiųjų. Tačiau būna ir specifinių nėščiųjų dermatozių. Joms priskiriami polimorfinis nėščiųjų bėrimas (PEP), gestacinis pemfigoidas, intrahepatinė nėščiųjų cholestazė, pustulinė nėščiųjų žvynelinė, atopinė nėščiųjų būklė.

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27

Ekiz, Özlem, Bilge Bülbül Şen, Emine Nur Rifaioğlu, Tuğba Şen, Esin Atik, and Asena Çiğdem Doğramacı. "Büllöz pemfigoidli hastalarda 3 yıllık gözlem: 29 olgu." TURKDERM 47, no. 2 (2013): 205–8. http://dx.doi.org/10.4274/turkderm.80664.

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28

Mirceska, Arsovska, Katerina Damevska, Viktor Simeonovski, Andrija Jović, and Danica Tiodorović. "Neurological and psychiatric comorbidities in bullous pemphigoid." Acta Facultatis Medicae Naissensis 39, no. 4 (2022): 476–83. http://dx.doi.org/10.5937/afmnai39-35922.

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Introduction: Bullous pemphigoid (BP) is an autoimmune skin disease that typically presents with severe itching and blistering, with or without eczematous and urticarial lesions. Patients with BP are at an increased risk of comorbid conditions, especially neurologic and psychiatric diseases. Several recent studies have found a link between BP and neurological disorders, especially stroke, dementia, and Parkinson's disease. The aim of our study was to evaluate the prevalence of neurological and psychiatric comorbidities and their treatment in BP patients. Methods: A cross-sectional, observation

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29

Bubilaitė, Agnė, Vesta Kučinskienė, Jurgita Makštienė, et al. "Sergančiųjų autoimuninėmis pūslinėmis ligomis klinikinės ir imunologinės charakteristikos. Pilotinis tyrimas." Lithuanian General Practitioner 27, no. 6 (2023): 306–11. http://dx.doi.org/10.37499/lbpg.1215.

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Autoimuninės pūslinės ligos (APL) – tai retų odos ligų grupė, kuriai būdingos pūslės ir erozijos odoje ir (arba) gleivinėse. Tikslas. Nustatyti sergančiųjų APL klinikines ir imunologines charakteristikas. Metodika. Atliktas perspektyvusis pilotinis tyrimas, į kurį įtraukti pacientai su pirmą kartą nustatyta ir negydyta APL, kai, atlikus odos arba gleivinės biopsiją, gautas teigiamas tiesioginės imunofluorescencijos (TIF) rezultatas. Rezultatai. Į tyrimą įtraukta 13 tiriamųjų (7 moterys, 6 vyrai), 10 iš 13 diagnozuotas pūslinis pemfigoidas (BP), 2 iš 13 – paraneoplastinė pūslinė (PP), 1 iš 13 –

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30

Palmela Pereira, Cristiana, Rui Santos, Leonor Ferreira, et al. "A 10-Year Observational Study on Treatment Approaches in Pemphigus and Pemphigoid." Acta Stomatologica Croatica 59, no. 2 (2025): 190–98. https://doi.org/10.15644/asc59/2/8.

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31

Cvetković Jordanov, Lidija, Lidija Kandolf Sekulović, Željko Mijušković, Lidija Zolotarevski, and Radoš Zečević. "Concomitant Psoriasis and Bullous Pemphigoid – a Case Report / Udružena pojava psorijaze i buloznog pemfigoida – prikaz slučaja." Serbian Journal of Dermatology and Venereology 6, no. 1 (2014): 30–38. http://dx.doi.org/10.2478/sjdv-2014-0003.

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Abstract Concomitant occurrence of psoriasis and bullous pemphigoid was described in less than 100 cases in the literature. The co-occurrence affects the treatment approach of patients. We present a case of a 58-year-old man with psoriasis presenting with erythematous plaques, tense bullae, erosions and fever up to 39°C. Direct and indirect immunofluorescence and histopathological examination confirmed the diagnosis of bullous pemphigoid. In our case, bullous eruptions were successfully treated with oral methylprednisolone and dapsone, and psoriasis with narrowband ultraviolet B phototherapy a

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32

Radičević, Miloš, and Snežana Minić. "Epidemiology and comorbidities in bullous pemphigoid in the period from January of 2019 to the January of 2021." Medicinski podmladak 73, no. 2 (2022): 40–46. http://dx.doi.org/10.5937/mp73-33455.

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Introduction: Bullous pemphigoid is an autoimmune bullous dermatosis that most commonly occurs in elderly patients. Due to its pathogenesis and treatment of the disease, it can also affect the development of comorbidities. Aim: Determination of comorbidities and their frequency in patients with bullous pemphigoid, as well as their distribution by sex and the estimation of the duration of dermatosis from the onset of symptoms to data collection. Material and methods: In the period from January 2019 to January 2021, a number of 80 patients was analyzed. Basic patient data (age, sex, time of illn

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33

Żychowska, Magdalena, Aleksandra Batycka-Baran, Jacek Szepietowski, and Wojciech Baran. "Dapsone – mechanism of action, safety of use and the role in the treatment of bullous pemphigoid according to current recommendations." Dermatology Review 2 (2016): 176–84. http://dx.doi.org/10.5114/dr.2016.59141.

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34

Stroynowska-Kosik, Jagoda, Magalena Pałdyna, and Ewelina Biało-Wójcicka. "Birt-Hogg-Dube syndrome coexisting with bullous pemphigoid and basal cell carcinoma." Dermatology Review 108, no. 6 (2021): 534–43. http://dx.doi.org/10.5114/dr.2021.114607.

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35

Benelli, Elisa, Giulia Camilla Demarin, Paola Corneli, Alessandro Gatti, and Stefano Martelossi. "Le bolle che non ti aspetti: un raro caso di pemfigo volgare in età pediatrica." Medico e Bambino Pagine elettroniche 26, no. 2 (2023): 21–24. http://dx.doi.org/10.53126/mebxxvif021.

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A healthy 15-year-old boy in full well-being presents with multiple ulcerative lesions with an erosive appearance at the level of the oral cavity and the nasal mucosa. Two months after the onset, vesicular lesions also appear on the skin. As pemphigus vulgaris is suspected, a biopsy of the oral mucosa is performed which shows suprabasal bubbles, which confirms the diagnosis. Direct immuno-fluorescence tests show the presence of IgG against the epidermal substance and immunoserological tests detect anti-desmoglein I and III autoantibodies. Oral steroid therapy is prescribed, showing initial goo

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36

Tampoia, Marilina, Antonietta Zucano, Nicola Bizzaro, et al. "Gli autoanticorpi anti-BP180 e anti-BP230 sono marcatori predittivi ma non equivalenti di severità di malattia e di remissione clinica nel pemfigoide bolloso." La Rivista Italiana della Medicina di Laboratorio - Italian Journal of Laboratory Medicine 7, no. 1 (2011): 42–48. http://dx.doi.org/10.1007/s13631-011-0007-y.

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37

Vitoreli, Bianca Campos, Galileu Olímpio Nunes, Andressa Barbosa Melo, et al. "Abordagem terapêutica das doenças autoimunes cutâneas." CONTRIBUCIONES A LAS CIENCIAS SOCIALES 17, no. 7 (2024): e8055. http://dx.doi.org/10.55905/revconv.17n.7-042.

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As doenças autoimunes cutâneas representam um grupo diversificado de condições caracterizadas pela resposta imune aberrante contra componentes da pele. Exemplos dessas doenças incluem o lúpus eritematoso cutâneo, a dermatite herpetiforme, o pemfigoide bolhoso, entre outras. A abordagem terapêutica destas doenças é desafiadora devido à sua complexidade e variabilidade clínica. O tratamento visa controlar os sintomas, minimizar os danos à pele e melhorar a qualidade de vida dos pacientes. O objetivo deste estudo é revisar e sintetizar as abordagens terapêuticas atuais para as doenças autoimunes

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38

Mighic, C. "SKIN MANIFESTATIONS IN PREGNANCY." Deutsche internationale Zeitschrift für zeitgenössische Wissenschaft 49 (February 1, 2023): 22–24. https://doi.org/10.5281/zenodo.7594751.

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Pregnancy is a physiological state that induces skin manifestations. The presence of the fetus in the womb produces responses in the maternal body outside the physiological limits and consequently leads to the appearance of some pathological manifestations. Their rational treatment requires specifying the etiology.Gestationes Pemphigoid is a rare, intensely itchy skin condition that occurs only in association with pregnancy. It appears in the second or third trimester of pregnancy. The Polymorphous Eruption of pregnancy usually affects first pregnancy in the third trimester or immediately post

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39

Boccomini, Carola, Marco Ladetto, Luigi Rigacci, et al. "Brief Chemoimmunotherapy Rituximab, Bendamustine, Mitoxantrone (R-BM) Followed by Rituximab Consolidation in Elderly Patients with Untreated Advanced Stage Follicular Lymphoma (FL): Preliminary Results of a Prospective Phase II Study by Fondazione Italiana Linfomi (FIL)." Blood 120, no. 21 (2012): 2720. http://dx.doi.org/10.1182/blood.v120.21.2720.2720.

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Abstract Abstract 2720 Introduction: Bendamustine is a promising agent that has been showed high efficacy in combination with Rituximab in indolent lymphomas; however experiences on its use in combination with other cytotoxic agents are scant, particularly in FL. A previous FIL trial showed that a brief R-FND induction chemoimmunotherapy with only 4 courses of R-chemotherapy followed by 4 rituximab doses as consolidation can achieve high CR and PFS rates in FL patients, supporting the feasibility of this regimen in the elderly (Vitolo et al, ASH 2011). These promising results prompted FIL to i

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40

COWAN, Timothy, Lucinda WALLMAN, and Dedee MURRELL. "Vaxzevria COVID-19 aşısı sonrasında gelişen şiddetli büllöz pemfigoid." Mucosa, November 13, 2021. http://dx.doi.org/10.33204/mucosa.993581.

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Pfizer ve Moderna COVID-19 aşılarına sekonder büllöz pemfigoid az sayıda olguda tanımlanmıştır. Bu, Oxford-AstraZeneca Vaxzevria COVID-19 aşısı tarafından tetiklenen bildirilmiş ilk büllöz pemfigoid vakasıdır. Olgunun ilk semptomları, aşının ilk dozundan dört hafta sonra ortaya çıkmış ve büllöz pemfigoid tanısı direkt immünofloresan test ve BP180 antikor pozitifliği ile doğrulanmıştır.

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Brahmanti, Herwinda, Nesa Wike Wilanti, Diah Prabawati Retnani, and Anny Setijo Rahaju. "TERAPI DAPSON PADA PEMFIGOID BULOSA." Media Dermato Venereologica Indonesiana 46, no. 3 (2019). http://dx.doi.org/10.33820/mdvi.v46i3.70.

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Pemfigoid bulosa (PB) merupakan penyakit autoimun bulosa subepidermis yang umumnya menyerang orang berusia di atas 70 tahun. Pemfigoid bulosa jarang ditemukan pada usia muda, tetapi penting untuk mempertimbangkan kemungkinan diagnosis PB pada kelompok usia ini. Pemeriksaan imunofluoresen langsung (DIF) bertujuan untuk mengamati deposit linear IgG dan C3 dalam zona membran basalis, terkait diagnosis banding PB dengan penyakit bulosa subepidermis lainnya. Dalam laporan kasus ini, perempuan berusia 26 tahun datang dengan keluhan utama lepuh berdinding tegang yang timbul di atas bercak merah yang

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Erdoğan, Bilgen, Zeynep Topkarcı, Murat Yılmaz, and Ayşe Kavak. "Büllöz pemfigoid ve nörolojik hastalıkların birlikteliği: retrospektif değerlendirme." Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy, December 15, 2012. http://dx.doi.org/10.5350/btdmjb201208403.

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kilinc, fahriye, ugur gulper, ilkay ozer, and ibrahim kilinc. "An Overview of The Results of Direct Immunofluorescence in Mucocutaneous Biopsies: Single Center Experience." Selcuk Tip Dergisi, September 1, 2023. http://dx.doi.org/10.30733/std.2023.01638.

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Amaç: Direkt immünfloresan ve histopatolojik inceleme yapılan cilt/mukoza biyopsilerinin immünfloresan sonuçlarını, histomorfolojik bulgularını, ön tanılarıyla uyumunu karşılaştırmak ve immünfloresan incelemenin diagnostik rolünü değerlendirmek amaçlanmıştır. Hastalar ve Yöntem: 01 Ocak 2019 – 31 Aralık 2019 tarihleri arasında patoloji laboratuvarına gönderilen toplam 207 hastanın biyopsileri değerlendirildi. Ön tanılara göre gruplar oluşturuldu, histolojik ve direkt immünfloresan bulgular kaydedildi. SPSS programında Kappa istatistikleri ve McNemar testi kullanıldı. P<0.05 istatistiksel ol

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SUBAŞI GÖKŞİN, Şule, and Işıl Göğem İMREN. "Retrospective Analysis of Skin Changes and Dermatoses Observed in Pregnants Applying to the Dermatology Outpatient Clinic." Harran Üniversitesi Tıp Fakültesi Dergisi, December 20, 2023, 649–56. http://dx.doi.org/10.35440/hutfd.1364998.

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Amaç: Gebelikte endokrinolojik, vasküler veya immünolojik değişiklikler deride birçok farklı klinik duruma neden olabilir. Dermatoloji polikliniğine başvuran gebe hastalarda gözlenen deri değişiklikleri ve dermatozların klinik analizini yapmak. Materyal ve metod: Çalışmaya Mart 2021 ile Eylül 2022 tarihleri arasında dermatoloji polikliniğine başvuran 112 gebe hasta dahil edildi. Bulgular: Hastaların yaş ortalaması 28,8±6.9 (min.18-max.44) idi. Gebelerin %58'i primigravida, %42'si multigravida idi. Gebeler sıklıkla 2. ve 3. trimesterde polikliniğe başvurdu (78.6%). Olguların %82.1'inde fizyoloj

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SUBAŞI GÖKŞİN, Şule, Buket ER URGANCI, Işıl Göğem İMREN, and İbrahim AÇIKBAŞ. "Büllöz pemfigoidli hastalarda serum ve lezyonel miRNA-1291 ekspresyonlarının karşılaştırılması." Pamukkale Medical Journal, September 15, 2022. http://dx.doi.org/10.31362/patd.1174388.

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Purpose: Bullous pemphigoid (BP) is an autoimmune disease increasing by age. miRNA-1291 is a microRNA that plays major role in many immune-mediated cutaneous diseases. We aimed to investigate the role of miRNA-1291 in BP by comparing its expression levels in serum and lesional skin and its correlation with other BP biomarkers (CCL17, anti-BP180, and anti-BP230). Materials and methods: Twenty three patients with BP and 23 healthy control patients were included in the study. The miRNeasy Mini Kits was used for RNA isolation from serum and biopsy samples. Qiagen-miRCURY LNA RT Kit was used

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