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Journal articles on the topic 'Schonlein purpura'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Retnaningtyas, Lucia Pudyastuti. "Henoch-Schonlein Purpura (HSP)." KELUWIH: Jurnal Kesehatan dan Kedokteran 1, no. 1 (2019): 19–26. http://dx.doi.org/10.24123/kesdok.v1i1.2486.

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Abstract—Henoch-Schonlein purpura (HSP) is a systemic vasculitic disease (vascular inflammation) characterized by the deposition of immune complexes consisting of IgA in kidney skin. This disease is called Anaphylactoid purpura, rheumatic Purpura, Schonlein-Henoch purpura. In this case, the patient complained of the appearance of red spots on the legs to the buttocks within three days and did not feel itchy. Ankle pain and can not be moved, and do not feel nausea, fever, heartburn, and others. Examination of the extremities contained red lesions and was more prominent than other skin surfaces.

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2

Sakharkar, Kanchan, Sunil N. Mhaske, Liza Bulsara, and R. B. Kothari. "Henoch Schonlein Purpura." Indian Journal of Trauma & Emergency Pediatrics 9, no. 2 (2017): 59–61. http://dx.doi.org/10.21088/ijtep.2348.9987.9217.10.

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3

Shi, Xiang, Wen-Chao Li, Li-Jun Mo, et al. "Altered mean platelet volume in children with Henoch-Schonlein purpura and its association with disease activity." Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 55, no. 3 (2017): 368–72. http://dx.doi.org/10.1177/0004563217727015.

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Background Henoch-Schonlein purpura is a systemic small-vessel vasculitis that occurs mainly in children. A review of the literature has suggested a correlation between mean platelet volume and several inflammatory disorders. However, to the best of our knowledge, any potential correlation between mean platelet volume and Henoch-Schonlein purpura has not been reported in the literature. Therefore, our study aimed to evaluate the role of mean platelet volume concentrations in patients with Henoch-Schonlein purpura. Methods This study included 97 children with Henoch-Schonlein purpura and 120 he

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4

Côté, Jean-Maxime, Rosalie-Sélène Meunier, Jan-Alexis Tremblay, Florence Weber, and Michèle Mahone. "Henoch-Schonlein purpura in pregnancy: A case report." Obstetric Medicine 11, no. 4 (2018): 195–97. http://dx.doi.org/10.1177/1753495x17745391.

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Henoch-Schonlein purpura is a relatively common pediatric vasculitis. Very few cases of Henoch-Schonlein purpura during pregnancy have been described. Henoch-Schonlein purpura is variable in its presentation, from completely benign to possibly catastrophic complications. This rarely encountered condition in adults can also be a recurrence of a previous childhood disease. We present a case of a pregnant 40-year-old woman with Henoch-Schonlein purpura, resulting in a viable birth with no fetal complications. Her presentation is discussed in detail and a general presentation of Henoch-Schonlein p

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Pudjiadi, Marissa Tania Stephanie, and Taralan Tambunan. "Nefritis Purpura Henoch Schonlein." Sari Pediatri 11, no. 2 (2016): 102. http://dx.doi.org/10.14238/sp11.2.2009.102-7.

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Nefritis Henoch-Schonlein adalah purpura Henoch Schonlein (PHS) dengan keterlibatan ginjal. Manifestasinefritis Henoch-Schonlein antara lain hematuria mikroskopik, hematuria makroskopis, proteinuria, sampaigagal ginjal kronik. Patogenesis PHS belum diketahui secara pasti, namun secara umum diakibatkan olehdeposisi imun kompleks akibat polimer IgA1 pada kulit, saluran gastrointestinal, dan kapiler glomerulus.Klasifikasi nefritis Henoch-Schonlein berdasarkan The International Study of Kidney Disease in Childrenterbagi atas enam kelas. Purpura Henoch Schonlein umumnya bersifat self-limiting dan h

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ROSENBLUM, NORMAN D., and HARLAND S. WINTER. "Steroid Effects on the Course of Abdominal Pain in Children With Henoch-Schonlein Purpura." Pediatrics 79, no. 6 (1987): 1018–21. http://dx.doi.org/10.1542/peds.79.6.1018.

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Henoch-Schonlein purpura is a systemic vasculitis of unknown cause that is characterized primarily by abdominal pain, arthritis, and purpuric skin lesions. Abdominal pain is the most common gastrointestinal symptom, but intestinal bleeding and intussusception may occur. Previous studies have supported the use of steroids in managing the abdominal pain of Henoch-Schonlein purpura.1,2 Because there are no controlled trials using steroids in this disease, their value in affecting the intestinal lesions of Henoch-Schonlein purpura remains unknown. The purpose of this retrospective study was to ass

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7

Lei, Wang, Shan Yun-Yun, and Xu Ai-E. "Neutrophil-to-lymphocyte Ratio: A Biomarker for Predicting Systemic Involvement in Henoch–Schonlein Purpura." Indian Journal of Dermatology, Venereology and Leprology 88 (September 1, 2021): 132. http://dx.doi.org/10.25259/ijdvl_760_19.

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Background: Henoch–Schonlein purpura (HSP) is one of the commonest entities included within the category of cutaneous vasculitis (CV). Our work is purposed to explore the predictive value of neutrophil-to-lymphocyte ratio (NLR) for systemic involvement in Henoch– Schonlein purpura patients. This ratio is known as an inflammatory marker, and is used to assess the systemic inflammation associated with various diseases. Our objective is to establish whether it can be applied for the prediction of renal and gastrointestinal (GI) or purely renal involvement in Henoch–Schonlein purpura. Aim: To dete

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8

Wijaya, Indriyani. "Anesthetic Management of A Patient with Henoch-Schonlein Purpura for Caesarean Section." Indonesian Journal of Anesthesiology and Reanimation 4, no. 2 (2022): 107–14. http://dx.doi.org/10.20473/ijar.v4i22022.107-114.

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Introduction: Henoch-Schonlein Purpura or Immunoglobulin-A vasculitis is a systemic vasculitis caused by immune complexes that attack small blood vessels. The classic symptoms of Henoch-Schonlein Purpura include erythema purpura, arthralgia, gastrointestinal complaints, and renal involvement. Some cases show that pregnancy itself could be the trigger for its recurrence and lead to early delivery. Case report: A 33-year-old patient, G2P1A0 and 35 weeks and 4 days pregnant complained of diarrhea 8 days before hospital admission (8-15 times per day). The patient was diagnosed with Henoch-Schonlei

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9

Narchi, H., T. J. Beattie, R. G. Taylor, T. J. Evans, and A. F. Azmy. "Pseudomembranous Colitis in Association with Henoch Schonlein Purpura." Scottish Medical Journal 33, no. 4 (1988): 308–9. http://dx.doi.org/10.1177/003693308803300410.

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We describe the occurrence of antibiotic-associated pseudomembranous colitis in two cases of Henoch Schonlein purpura. We discuss the potential diagnostic difficulties and suggest that Henoch Schonlein purpura may predispose to the development of antibiotic-associated pseudomembranous colitis.

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10

Dehghanmehr, Sadegh, Reza Naghdi, Farahnaz Irandegani, Hamed Taheri, Omar Pourbalouch, and Ferdows Bamari. "Epidemiological Study of Henoch-Schonlein Purpura and its Characteristics in Infected Children During 2009-2016." Pakistan Journal of Medical and Health Sciences 15, no. 6 (2021): 1629–33. http://dx.doi.org/10.53350/pjmhs211561629.

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Introduction: Due to the different complications caused by Henoch-Schonlein purpura and in order to prevent additional treatment costs for patients, we decided to investigate the clinical features of cases of Henoch-Schonlein purpura. Materials and Methods: In this descriptive cross-sectional study, 52 children in whom the diagnosis of Henoch-Schonlein purpura was confirmed were enrolled in the study from 2009 to 2016. The instruments of this research include a researcher-made questionnaire with two parts. The first part is related to demographic characteristics including age, sex and season o

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11

Reid-Adam, J. "Henoch-Schonlein Purpura." Pediatrics in Review 35, no. 10 (2014): 447–49. http://dx.doi.org/10.1542/pir.35-10-447.

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12

Tizard, E. J. "Henoch-Schonlein purpura." Archives of Disease in Childhood 80, no. 4 (1999): 380–83. http://dx.doi.org/10.1136/adc.80.4.380.

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13

Ballinger, Susan. "Henoch-Schonlein purpura." Current Opinion in Internal Medicine 2, no. 6 (2003): 636–39. http://dx.doi.org/10.1097/00132980-200302060-00016.

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14

Ballinger, Susan. "Henoch-Schonlein purpura." Current Opinion in Internal Medicine 2, no. 6 (2003): 636–39. http://dx.doi.org/10.1097/00132980-200312000-00016.

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15

Barraza, Luis, Yecheskel Schneider, Randy Longman, David Wan, and Ellen J. Scherl. "Henoch-Schonlein Purpura." American Journal of Gastroenterology 111 (October 2016): S1010. http://dx.doi.org/10.14309/00000434-201610001-02114.

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16

CHATTERJEE, T., and DAWA SAMDUP. "HENOCH SCHONLEIN PURPURA." Medical Journal Armed Forces India 56, no. 1 (2000): 85–86. http://dx.doi.org/10.1016/s0377-1237(17)30107-7.

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17

Tizard, E. J., and M. J. J. Hamilton-Ayres. "Henoch Schonlein purpura." Archives of Disease in Childhood - Education and Practice 93, no. 1 (2008): 1–8. http://dx.doi.org/10.1136/adc.2004.066035.

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18

Szer, Ilona S. "Henoch-Schonlein purpura." Current Opinion in Rheumatology 6, no. 1 (1994): 25–31. http://dx.doi.org/10.1097/00002281-199401000-00005.

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19

Ballinger, Susan. "Henoch–Schonlein purpura." Current Opinion in Rheumatology 15, no. 5 (2003): 591–94. http://dx.doi.org/10.1097/00002281-200309000-00012.

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20

Heng, Madalene C. Y. "HENOCH-SCHONLEIN PURPURA." British Journal of Dermatology 112, no. 2 (1985): 235–40. http://dx.doi.org/10.1111/j.1365-2133.1985.tb00089.x.

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21

Moore, S., A. Bowden, and S. Afify. "Henoch--Schonlein purpura." Case Reports 2011, feb21 2 (2011): bcr0720103132. http://dx.doi.org/10.1136/bcr.07.2010.3132.

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22

Tarvin, S. E., and Susan Ballinger. "Henoch–Schonlein purpura." Current Paediatrics 16, no. 4 (2006): 259–63. http://dx.doi.org/10.1016/j.cupe.2006.05.003.

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23

Qin, Shuai, Dan Li, and Bo Zhang. "Analysis of Nursing Effect of Children with Henoch-Schonlein Purpura Based on the PDCA Nursing Model." Computational and Mathematical Methods in Medicine 2021 (December 13, 2021): 1–8. http://dx.doi.org/10.1155/2021/1736429.

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By applying the PDCA model to the care of children with Henoch-Schonlein purpura, the nursing process can be divided into four stages: planning, execution, inspection, and treatment. According to the age characteristics and disease progression of pediatric patients, a complete nursing plan is formulated to efficiently implement the nursing content and improve the nursing effect. This paper studies the application of the PDCA nursing model in the nursing of children with Henoch-Schonlein purpura and statistically analyzes the disappearance of skin rash, joint pain relief, disappearance of urine

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24

Abbas, Shanavas, Geetha S., Deepthi R.V., Jubin Kamar, and Susan Uthup. "Clinical profile and outcome of Henoch Schonlein purpura in a tertiary care hospital in South India." International Journal of Contemporary Pediatrics 4, no. 3 (2017): 822. http://dx.doi.org/10.18203/2349-3291.ijcp20171493.

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Background: Henoch Schonlein purpura (HSP) is the most common systemic vasculitis in children. It is an immunoglobulin A (IgA) mediated systemic small-vessel vasculitis, with IgA deposition in vessel walls leading to symptoms involving the skin, joints, intestines, and kidneys. The objective of present study was to identify and describe the clinical profile, pattern of joint involvement, histopathological features, treatment modalities and complications of Henoch Schonlein purpura.Methods: 52 children less than 12 years diagnosed to have Henoch Schonlein Purpura according to the European Leagu

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25

Kassam, Farah, Sabrina Nurmohamed, and Richard M. Haber. "Koebner phenomenon in leukocytoclastic vasculitis: A case report and an updated review of the literature." SAGE Open Medical Case Reports 7 (January 2019): 2050313X1985035. http://dx.doi.org/10.1177/2050313x19850353.

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Leukocytoclastic vasculitis is the most common form of cutaneous vasculitis. It is a neutrophilic small vessel vasculitis resulting from the deposition of circulating immune complexes. Henoch-Schonlein purpura is a systemic type of leukocytoclastic vasculitis, characterized by immunoglobulin A-mediated blood vessel injury. We present a case of Henoch-Schonlein purpura in an adult female manifesting with a vasculitic rash with Koebner phenomenon.

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26

Nguyen-Ho, Phong, Laurence D. Jewell, and Alan BR Thomson. "Hemorrhagic Intestinal Henoch-Schonlein Purpura Complicated by Cytomegalovirus Infection." Canadian Journal of Gastroenterology 12, no. 1 (1998): 71–74. http://dx.doi.org/10.1155/1998/896945.

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A 54-year-old man on hemodialysis for acute chronic renal failure and on corticosteroids for Henoch-Schonlein purpura developed massive hematochezia. After extensive clinical investigation, an ileal bleeding site was identified and surgically removed. Pathological examination of the diseased bowel segment revealed an extensive vasculitis with mucosal ulceration attributable to Henoch-Schonlein purpura as well as florid cytomegalovirus infection.

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27

Wong, Christina T., and John W. Harrington. "Infantile Henoch-Schonlein purpura." Emergency Medicine Australasia 16, no. 3 (2004): 225–28. http://dx.doi.org/10.1111/j.1742-6723.2004.00591.x.

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28

Fervenza, Fernando C. "Henoch-Schonlein purpura nephritis." International Journal of Dermatology 42, no. 3 (2003): 170–77. http://dx.doi.org/10.1046/j.1365-4362.2003.01769.x.

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29

Shetty, A. K. "Infantile Henoch-Schonlein Purpura." Archives of Family Medicine 9, no. 6 (2000): 553–56. http://dx.doi.org/10.1001/archfami.9.6.553.

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30

Zhou, Fang, Qimin Shao, Lihong Jia, and Chunyan Cai. "Gut Microbiota Variations between Henoch-Schonlein Purpura and Henoch-Schonlein Purpura Nephritis." Gastroenterology Research and Practice 2022 (April 14, 2022): 1–7. http://dx.doi.org/10.1155/2022/4003491.

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Background. In China, little is known regarding the differences between children with Henoch-Schonlein purpura (HSP) and Henoch-Schonlein purpura nephritis (HSPN) concerning their gut microbiota. Methods. We recruited 25 children with HSP, 25 children with HSPN, and 25 healthy children to investigate the differences. Fecal samples were collected and analyzed by sequencing the V3-V4 region of the 16S rRNA gene. The diversity of the fecal gut microbiota was compared between the patient groups. Results. Rarefaction curves showed that the gut microbial diversity between the three groups differed s

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31

Markin, Leonid, and Olena Rachkevych. "HEMORRHAGIC VASCULITIS (HENOCH-SCHONLEIN PURPURA) IN PREGNANCY: LITERATURE REVIEW AND CASE REPORT." Acta Medica Leopoliensia 27, no. 3-4 (2021): 52–58. http://dx.doi.org/10.25040/aml2021.3-4.052.

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Aim. The paper aims at reviewing publications and analyzing a clinical case of Henoch-Schonlein purpura in a pregnant patient. This pathology is extremely rare in pregnancy (solely about 20 cases reported in the available literature) Materials and Methods. A systematic literature search was performed in Pubmed and other sources on peculiarities of gestation in Henoch-Schonlein purpura. A case of Henoch-Schonlein purpura in a pregnant woman, who delivered in 2020 in Lviv Maternity Hospital №1 is presented. Results and Discussion. Henoch-Shonlein purpura is extremely rare disease in

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32

Research and Practice, Gastroenterology. "Retracted: Gut Microbiota Variations between Henoch-Schonlein Purpura and Henoch-Schonlein Purpura Nephritis." Gastroenterology Research and Practice 2023 (December 20, 2023): 1. http://dx.doi.org/10.1155/2023/9840245.

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33

Payton, C. D., M. E. M. Allison, and J. M. Boulton-Jones. "Henoch Schonlein Purpura Presenting with Pulmonary Haemorrhage." Scottish Medical Journal 32, no. 1 (1987): 26–27. http://dx.doi.org/10.1177/003693308703200113.

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A young woman presented with arthralgia, a rash and dramatic haemoptysis, and renal involvement was indicated by proteinuria, haematuria and a rising serum creatinine. A systemic vasculitic disorder was suspected initially, but the diagnosis of Henoch-Schonlein purpura was established by the finding of mesangial IgA deposits on renal biopsy. Immunofluorescent study of renal biopsy material is vital to diagnosis where the clinical features of Henoch-Schonlein purpura and those of the systemic vasculitides with renal involvement prove to be indistinguishable.

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34

Asiri, Ashwag, Faris Alzahrani, Salem Alshehri, and Yossef Hassan AbdelQadir. "New-Onset Henoch–Schonlein Purpura after COVID-19 Infection: A Case Report and Review of the Literature." Case Reports in Pediatrics 2022 (March 29, 2022): 1–5. http://dx.doi.org/10.1155/2022/1712651.

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Extrapulmonary manifestations of COVID-19 infection include a wide spectrum of cutaneous, endocrine, and cardiovascular complications. We report three cases of new-onset Henoch–Schonlein purpura (HSP) in COVID-19 infected children that were diagnosed and treated in Abha Maternity and Children Hospital, Saudi Arabia, between 28th July 2020 and 10th August 2020. All three cases were males younger than 5 years of age that presented with Henoch–Schonlein purpura characteristic rash and arthralgia without a recent history of any infection, especially respiratory infections. They all tested positive

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35

Prince, Shah, Buddhadev Mohit, P. SRINIVAS NAYAK S, and Chakraborthy Gunosindhu. "A Case Report on Henoch-Schonlein Purpura." OPEN JOURNAL OF CASE REPORTS 2, no. 7 (2021): 1–3. https://doi.org/10.5281/zenodo.5598681.

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Henoch-Schonlein purpura (HSP) also known as IgA vasculitis is a disorder that causes the small blood vessels in your skin, joints, intestines, and kidneys to become inflamed and bleed. The most striking feature of this form of vasculitis is a purplish rash, typically on the lower legs and buttocks. Henoch-Schonlein purpura can also cause abdominal pain. This case report describes a 13 year old female patient presented with complains of Rashes over both upper and lower limb, black stool, blood in urine since last 10 days, swelling over both limbs. Other complaints included blood in vomit. diag

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36

Tanju, Ilhan Asya, Ozgur Pirgon, Ferhat Cekmez, and Ferhan Karademir. "Diabetic Ketoacidosis Precipitated by Henoch-Schonlein Purpura." International Journal of Biomedical Science 5, no. 2 (2009): 189–91. http://dx.doi.org/10.59566/ijbs.2009.5189.

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Numerous investigations have been devoted to the search for environmental factors controlling the onset of autoimmune diseases. Pancreatic involvement, a rare complication of Henoch-Schonlein purpura, has been found mainly in adults, and it has not been reported in children. We present a case of a severe diabetic ketoacidosis in a child, a 7-year-old boy, following a typical clinical picture of Henoch-Schonlein purpura. Therapy with intravenous insulin resulted in resolution of the diabetic ketoacidosis and resolved the petechial rash of both legs.

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37

Chen, Winnie Arnissa, and Ity Sulawati. "HENOCH SCHONLEIN PURPURA PADA ANAK : LAPORAN KASUS." PREPOTIF : JURNAL KESEHATAN MASYARAKAT 8, no. 3 (2024): 7677–84. https://doi.org/10.31004/prepotif.v8i3.38543.

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Henoch schonlein purpura yang dikenal juga sebagai immunoglobulin A vasculitis (IgAV) merupakan inflamasi pada pembuluh darah kecil sistemik yang diperantarai imunoglobulin A (IgA), dengan pengendapan IgA di dinding pembuluh darah kecil di kulit, sendi, saluran pencernaan dan ginjal, dapat pula melibatkan sistem saraf pusat dan paru-paru tetapi jarang terjadi. Penyakit ini merupakan kelainan akut yang diperantarai IgA dan biasanya dapat sembuh dengan sendirinya apabila ditangani dengan perawatan suportif. Seorang anak perempuan berusia 11 tahun datang ke RSUD Ciawi dengan keluhan utama nyeri p

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38

Oner, Ayse, and Gulay Demircin. "Henoch Schonlein Purpura in Childhood." Current Pediatric Reviews 1, no. 2 (2005): 161–72. http://dx.doi.org/10.2174/1573396054065510.

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39

Lee, Young J. "Danazol for Henoch-Schonlein Purpura." Annals of Internal Medicine 118, no. 10 (1993): 827. http://dx.doi.org/10.7326/0003-4819-118-10-199305150-00021.

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40

Stamenković, Hristina, Tatjana Stanković, and Zlatko Đurić. "HENOCH-SCHONLEIN PURPURA IN CHILDHOOD." Acta Medica Medianae 54, no. 4 (2015): 32–36. http://dx.doi.org/10.5633/amm.2015.0405.

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41

Cummins, D. L., D. Mimouni, A. Rencic, D. J. Kouba, and C. H. Nousari. "Henoch-Schonlein purpura in pregnancy." British Journal of Dermatology 149, no. 6 (2003): 1282–85. http://dx.doi.org/10.1111/j.1365-2133.2003.05671.x.

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42

Kalmantis, K., G. Daskalakis, C. Iavazzo, A. Vranos, S. Mesogitis, and A. Antsaklis. "Henoch–Schonlein purpura in pregnancy." Journal of Obstetrics and Gynaecology 28, no. 4 (2008): 403–5. http://dx.doi.org/10.1080/01443610802091990.

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43

Johnson, Pamela T., Karen M. Horton, and Elliot K. Fishman. "Case 127: Henoch-Schonlein Purpura." Radiology 245, no. 3 (2007): 909–13. http://dx.doi.org/10.1148/radiol.2453040999.

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KIM, EUN JUNG, HYUNG JIK KIM, SEOUNG GYUN KIM, et al. "ALOE-INDUCED HENOCH?SCHONLEIN PURPURA." Nephrology 12, no. 1 (2007): 109. http://dx.doi.org/10.1111/j.1440-1797.2006.00752.x.

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45

Kamath, Nutan, and Suchetha Rao. "Henoch–Schonlein purpura: An update." Indian Journal of Rheumatology 7, no. 1 (2012): 92–98. http://dx.doi.org/10.1016/s0973-3698(12)60034-x.

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46

Lind, J., A. Mackay, and SJ Withers. "Henoch-Schonlein purpura and priapism." Journal of Paediatrics and Child Health 38, no. 5 (2002): 526–27. http://dx.doi.org/10.1046/j.1440-1754.2002.00028.x.

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47

Saulsbury, F. T. "Epidemiology of Henoch-Schonlein purpura." Cleveland Clinic Journal of Medicine 69, Suppl_2 (2002): SII87. http://dx.doi.org/10.3949/ccjm.69.suppl_2.sii87.

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48

Sarma, P. S. "Dapsone in Henoch-Schonlein purpura." Postgraduate Medical Journal 70, no. 824 (1994): 464–65. http://dx.doi.org/10.1136/pgmj.70.824.464.

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49

Kaila, Vishal, Nivedita Sudhekar, and Mark Feldman. "2658 Henoch-Schonlein Purpura Duodenitis." American Journal of Gastroenterology 114, no. 1 (2019): S1463. http://dx.doi.org/10.14309/01.ajg.0000600164.46571.bd.

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50

Arora, Mrinal, and Alpana Prasad. "Henoch Schonlein Purpura: Unusual presentation." Current Medicine Research and Practice 6, no. 1 (2016): 43–44. http://dx.doi.org/10.1016/j.cmrp.2016.01.003.

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