Systemic Lupus Erythematosus with Multiple Autoimmune Disease Presented with Extensive Peripheral Gangrene

Author:

Alzughayyar Tareq Z.1ORCID,Zalloum Jihad Samer1ORCID,Elqadi Mohammad N.1ORCID,Abukhalaf Sadi A.1ORCID,Abunejma Fawzy M.2,Alkhanafsa Mohammed M. Y.1,Haif Motasem H. M.1ORCID,Alqarajeh Firas1ORCID,Mesk Mo’min R.1ORCID,Misk Rami A.3ORCID

Affiliation:

1. Al-Quds University, Faculty of Medicine, Jerusalem, State of Palestine

2. Pediatric Rheumatologist, Al-Ahli Hospital, Hebron, State of Palestine

3. An-Najah National University, Faculty of Medicine & Health Sciences, Nablus, State of Palestine

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease and can be associated with other autoimmune diseases. SLE usually presents with skin change and rarely presents with gangrene. SLE gangrene usually involves the digits of upper extremities. We report the first case of SLE associated with an extremely rare constellation of neuromyelitis Optica (NMO) and diabetes mellitus type 1, presented with a rare form of the SLE gangrene which involves bilateral lower extremities up to midlegs, a case that has not yet been reported in the literature. Although SLE gangrene may respond to immunosuppressants, it has a high risk of complications that can end up with amputations.

Publisher

Wiley

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