A rare case of bilateral cystoid macular oedema associated with decompensated Henoch-Schonlein purpura-related nephropathy

2015 ◽  
Vol 44 (3) ◽  
pp. 209-212 ◽  
Author(s):  
Rajan S Patheja ◽  
Aaron Chidgey
Keyword(s):  
Macular Oedema ◽  
Rare Case ◽  
Cystoid Macular Oedema ◽  
Henoch Schonlein Purpura ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

A rare case of Henoch-Schönlein purpura with neurological involvement

2010 ◽  
Vol 40 (11) ◽  
pp. 795-796 ◽  
Author(s):  
E. Fiaux ◽  
Y. Benhamou ◽  
N. Cailleux ◽  
H. Levesque
Keyword(s):  
Rare Case ◽  
Neurological Involvement ◽  
Henoch Schonlein Purpura ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

scholarly journals A Rare Case of Helicobacter pylori Infection Complicated by Henoch-Schonlein Purpura in an Adult Patient

2020 ◽  
Vol 11 (6) ◽  
pp. 160-165
Author(s):  
Mujtaba Mohamed ◽  
Mohammed Shariff ◽  
Alsadiq Al Hillan ◽  
Rani Al Haj ◽  
Christian Kaunzinger ◽  
...  
Keyword(s):  
Helicobacter Pylori ◽  
Adult Patient ◽  
Rare Case ◽  
Helicobacter Pylori Infection ◽  
Henoch Schonlein Purpura ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

Henoch Schonlein Purpura Mimicking Lupus Nephritis-A Rare Case

2015 ◽  
Vol 4 (4) ◽  
pp. 81
Author(s):  
Amieleena Chhabra ◽  
Taoas Baikar ◽  
Vivek Dewan ◽  
tribhuvan Yadav
Keyword(s):  
Lupus Nephritis ◽  
Rare Case ◽  
Henoch Schonlein Purpura ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

scholarly journals Stroke and skin rash: A rare case of Henoch-Schonlein purpura

2012 ◽  
Vol 15 (4) ◽  
pp. 307 ◽  
Author(s):  
Kaushik Ghosh ◽  
JyotiTanmay Sau ◽  
Atri Chatterjee ◽  
Sandip Dey
Keyword(s):  
Skin Rash ◽  
Rare Case ◽  
Henoch Schonlein Purpura ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

scholarly journals A RARE CASE OF RECURRENT HENOCH-SCHONLEIN PURPURA IN AN ADULT

2021 ◽  
pp. 1
Author(s):  
Pardha Sivakoti ◽  
Saraswathi Banavath ◽  
Alekya Vulpala ◽  
Monica Rayapu ◽  
Bhagyaraj Pulavarthi ◽  
...  
Keyword(s):  
Rare Case ◽  
Henoch Schonlein Purpura ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

scholarly journals ADULT ONSET HENOCH: SCHONLEIN PURPURA – AN UNUSUAL PRESENTATION

2017 ◽  
Vol 10 (10) ◽  
pp. 2
Author(s):  
Srujith Chandrakanti ◽  
Oshin Mantro ◽  
Jagadeesan Mohanan ◽  
Mervin Kayipirambil Soman ◽  
Prasanna Karthik Suthakaran ◽  
...  
Keyword(s):  
Rare Case ◽  
Early Recognition ◽  
Leukocytoclastic Vasculitis ◽  
Renal Involvement ◽  
Unusual Presentation ◽  
Organ Involvement ◽  
Adult Onset ◽  
Henoch Schonlein Purpura ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

  Henoch–Schonlein purpura (HSP) is a common leukocytoclastic vasculitis seen in children. However, it is uncommon in adults. HSP is characterized by the classic tetrad of non-thrombocytopenic palpable purpura, arthritis or arthralgias, gastrointestinal, and renal involvement. We report a rare case of adult onset HSP with multi-organ involvement. Early recognition of multi-organ involvement is very important, especially in adults.

scholarly journals A Rare Case of Henoch-Schönlein Purpura Following a COVID-19 Vaccine—Case Report

2021 ◽  
Author(s):  
Abdelhamid Naitlho ◽  
Wahib Lahlou ◽  
Abderrahim Bourial ◽  
Hamza Rais ◽  
Nabil Ismaili ◽  
...  
Keyword(s):  
Case Report ◽  
Side Effects ◽  
Rare Case ◽  
Clinical Signs ◽  
Henoch Schonlein Purpura ◽  
Old Adult ◽  
Schonlein Purpura ◽  
Purpuric Rash ◽  
Henoch Schönlein Purpura ◽  
Rapid Regression

AbstractIn the COVID-19 pandemic era, anti-SARS-CoV-2 vaccination is considered to be the most efficient way to overtake the COVID-19 scourge. Like all medicines, vaccines are not devoid of risks and can in rare cases cause some various side effects. The objective of this case report is to highlight this unusual presentation of Henoch-Schönlein purpura following an anti-COVID-19 vaccination in a 62-year-old adult. The 62-year-old patient admitted to the emergency room for a petechial purpuric rash, sloping, occurring within hours, involving both legs and ascending. The clinical signs also included polyarthralgia and hematuria. Reported in the history the notion of an anti-COVID-19 vaccination 8 days prior to the onset of symptomatology. In the case of our patient, we retain the diagnosis of rheumatoid purpura based on the EULAR/PRINTO/PReS diagnostic criteria. Corticosteroid therapy (prednisone) was started, resulting to a rapid regression of clinical and laboratory symptoms, few days after the treatment. Patient was asymptomatic on subsequent visits. The low number of published cases of post-vaccine vasculitis does not question the safety of vaccines, but knowledge of such complications deserves to be known in order to avoid new immunizations that could have more serious consequences, and to avoid aggravating or reactivating a pre-existing vasculitis.

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