Skin Findings in a Patient with Sjogren’s Syndrome

Hypergammaglobulinemic purpura (HGP) is a syndrome constellating recurrent purpura, hypergammaglobulinemia, positive rheumatoid factor (RF), anti-Ro/La antibodies, and elevated erythrocyte sedimentation rate (ESR). We present a case of a 29-year-old female who was diagnosed with Sjogren’s syndrome f...

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Main Authors: Prajwal Boddu, Abdul S. Mohammed, Sonali Khandelwal
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Rheumatology
Online Access:http://dx.doi.org/10.1155/2016/4829459
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author Prajwal Boddu
Abdul S. Mohammed
Sonali Khandelwal
author_facet Prajwal Boddu
Abdul S. Mohammed
Sonali Khandelwal
author_sort Prajwal Boddu
collection DOAJ
description Hypergammaglobulinemic purpura (HGP) is a syndrome constellating recurrent purpura, hypergammaglobulinemia, positive rheumatoid factor (RF), anti-Ro/La antibodies, and elevated erythrocyte sedimentation rate (ESR). We present a case of a 29-year-old female who was diagnosed with Sjogren’s syndrome four years prior to presenting with rash on her lower extremities for a period of 6 months. Skin biopsy at the initial visit was consistent with leukocytoclastic vasculitis and was initiated on treatment for it. Her rash evolved into 2–5 mm scattered purpurae while she was on the treatment and a repeat biopsy showed extravasation of RBCs, a sparse mononuclear infiltrate with deposition of plasma cells, and no evidence of leukocytoclastic vasculitis, thus showing a transition from neutrophilic to mononuclear inflammatory vascular disease which is a rare occurrence. Hypergammaglobulinemic purpura sometimes turns out to be a challenging disease to manage and requires an integrated effort from the primary care doctors, rheumatologist, and dermatologist.
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spelling doaj-art-45d898dff6644074a53fe5bb3957a88b2025-02-03T07:24:59ZengWileyCase Reports in Rheumatology2090-68892090-68972016-01-01201610.1155/2016/48294594829459Skin Findings in a Patient with Sjogren’s SyndromePrajwal Boddu0Abdul S. Mohammed1Sonali Khandelwal2Advocate Illinois Masonic Medical Center, Department of Internal Medicine, 856 West Nelson Street, Apt No. 2002, Chicago, IL 60657, USAAdvocate Illinois Masonic Medical Center, Department of Internal Medicine, 2356 North Elston Avenue, No. 306, Chicago, IL 60614, USARUSH University Medical Center, Department of Rheumatology, 1725 West Harrison Street, Chicago, IL 60612, USAHypergammaglobulinemic purpura (HGP) is a syndrome constellating recurrent purpura, hypergammaglobulinemia, positive rheumatoid factor (RF), anti-Ro/La antibodies, and elevated erythrocyte sedimentation rate (ESR). We present a case of a 29-year-old female who was diagnosed with Sjogren’s syndrome four years prior to presenting with rash on her lower extremities for a period of 6 months. Skin biopsy at the initial visit was consistent with leukocytoclastic vasculitis and was initiated on treatment for it. Her rash evolved into 2–5 mm scattered purpurae while she was on the treatment and a repeat biopsy showed extravasation of RBCs, a sparse mononuclear infiltrate with deposition of plasma cells, and no evidence of leukocytoclastic vasculitis, thus showing a transition from neutrophilic to mononuclear inflammatory vascular disease which is a rare occurrence. Hypergammaglobulinemic purpura sometimes turns out to be a challenging disease to manage and requires an integrated effort from the primary care doctors, rheumatologist, and dermatologist.http://dx.doi.org/10.1155/2016/4829459
spellingShingle Prajwal Boddu
Abdul S. Mohammed
Sonali Khandelwal
Skin Findings in a Patient with Sjogren’s Syndrome
Case Reports in Rheumatology
title Skin Findings in a Patient with Sjogren’s Syndrome
title_full Skin Findings in a Patient with Sjogren’s Syndrome
title_fullStr Skin Findings in a Patient with Sjogren’s Syndrome
title_full_unstemmed Skin Findings in a Patient with Sjogren’s Syndrome
title_short Skin Findings in a Patient with Sjogren’s Syndrome
title_sort skin findings in a patient with sjogren s syndrome
url http://dx.doi.org/10.1155/2016/4829459
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AT sonalikhandelwal skinfindingsinapatientwithsjogrenssyndrome