scholarly journals Dehydrated Human Amnion/Chorion Membrane Allograft for Treatment of Recalcitrant Pyoderma Gangrenosum in PASH Syndrome and Systemic Lupus Erythematosus

2021 ◽  
Vol 5 (1) ◽  
Author(s):  
Weissman Amanda S ◽  
Patel Viral Sanjay ◽  
Moore Walter
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Pyoderma Gangrenosum ◽  
Lupus Erythematosus ◽  
Systemic Lupus ◽  
Human Amnion

Acquired ichthyosis and pyoderma gangrenosum in a patient with systemic lupus erythematosus

1993 ◽  
Vol 18 (3) ◽  
pp. 268-270 ◽  
Author(s):  
D. ROGER ◽  
J. C. ALDIGIER ◽  
P. PEYRONNET ◽  
J. M. BONNETBLANC ◽  
C. LEROUX-ROBERT
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Pyoderma Gangrenosum ◽  
Lupus Erythematosus ◽  
Systemic Lupus

Pyoderma Gangrenosum Mimicking Antiphospholipid Antibody Syndrome in a Child With Juvenile Systemic Lupus Erythematosus

2020 ◽  
Author(s):  
metin kaya gürgöze ◽  
Aslıhan Kara ◽  
Mehmet yusuf sarı ◽  
İlknur Çalık ◽  
Saadet Akarsu
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Skin Biopsy ◽  
Pyoderma Gangrenosum ◽  
Lupus Erythematosus ◽  
Anticoagulation Therapy ◽  
Anticardiolipin Antibody ◽  
Antiphospholipid Antibody ◽  
Antiphospholipid Antibody Syndrome ◽  
Systemic Lupus ◽  
History Of

Abstract Background: Although pyoderma gangrenosum (PG) -like lesions have been rarely described in adults with the antiphospholipid antibody syndrome (APS) and systemic lupus erythematosus (SLE), the occurrence of PG as a preceding manifestation of APS in children with SLE has not been reported until. We present a young girl with SLE and APS who developed progressive extstensive ulcerations that were consistent with PG.Case presentation: A 14-year-old girl with a 2-year history of SLE was admitted to our department, complaining painful crusted ulcerations on her legs. Skin biopsy was reported as PG. However, she did not respond to immunosuppressive therapy administered. When her skin biopsy findings is reassessed in keeping with the positive anticardiolipin antibody results, superficial small vessel microthrombosis was observed. Diagnosis of APS and PG developing secondary to SLE were made. It was resulted in marked clinical improvement with anticoagulation therapy in addition to immunosuppressives as is recommended in APS. Conclusions: Based in clinical, pathological and response to proposed treatment, we can state that PG -like lesions in children with SLE could be considered as a secondary form of APS.

scholarly journals Two case reports of pyoderma gangrenosum and systemic lupus erythematosus

Medicine ◽  
2018 ◽  
Vol 97 (34) ◽  
pp. e11933 ◽  
Author(s):  
Delphine Lebrun ◽  
Ailsa Robbins ◽  
Maxime Hentzien ◽  
Ségolène Toquet ◽  
Julie Plee ◽  
...  
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Pyoderma Gangrenosum ◽  
Lupus Erythematosus ◽  
Case Reports ◽  
Systemic Lupus

Systemic lupus erythematosus presenting as pyoderma gangrenosum in two cases

2008 ◽  
Vol 29 (7) ◽  
pp. 837-840 ◽  
Author(s):  
Seval Pehlevan Masatlıoğlu ◽  
Fatih Göktay ◽  
Ayşe Tülin Mansur ◽  
Ayşe Deniz Akkaya ◽  
Pembegül Güneş
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Pyoderma Gangrenosum ◽  
Lupus Erythematosus ◽  
Systemic Lupus

Pyoderma gangrenosum and systemic lupus erythematosus: a report of five cases and review of the literature

Lupus ◽  
2014 ◽  
Vol 24 (2) ◽  
pp. 130-137 ◽  
Author(s):  
J González-Moreno ◽  
M Ruíz-Ruigomez ◽  
J L Callejas Rubio ◽  
R Ríos Fernández ◽  
N Ortego Centeno
Keyword(s):  
Systemic Lupus Erythematosus ◽  
Pyoderma Gangrenosum ◽  
Lupus Erythematosus ◽  
Review Of The Literature ◽  
Systemic Lupus
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