A Man with Rapidly Progressive Limb Gangrene

Antiphospholipid syndrome (APS) and polyarteritis nodosa (PAN) are two distinct, but potentially overlapping, autoimmune disorders that are characterized by vascular morbidities. We present a case of probable APS that manifested as rapidly progressive peripheral gangrene with a positive test for lup...

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Main Authors: Ada Wing Tung Leung, Virginia Weng Nga Lao
Format: Article
Language:English
Published: World Scientific Publishing 2024-12-01
Series:Journal of Clinical Rheumatology and Immunology
Subjects:
Online Access:https://www.worldscientific.com/doi/10.1142/S2661341724720039
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author Ada Wing Tung Leung
Virginia Weng Nga Lao
author_facet Ada Wing Tung Leung
Virginia Weng Nga Lao
author_sort Ada Wing Tung Leung
collection DOAJ
description Antiphospholipid syndrome (APS) and polyarteritis nodosa (PAN) are two distinct, but potentially overlapping, autoimmune disorders that are characterized by vascular morbidities. We present a case of probable APS that manifested as rapidly progressive peripheral gangrene with a positive test for lupus anticoagulant (LAC), alongside with angiographic evidence of suspected renal and hepatic artery aneurysms commonly associated with PAN, but also the presence of diffuse thrombosis over the distal arterial branches in the four limbs. Through this case, we aim to review the overlapping features and potential interplay between APS and PAN, highlighting the necessary considerations for optimizing management to salvage the ongoing limb ischemia.
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publisher World Scientific Publishing
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series Journal of Clinical Rheumatology and Immunology
spelling doaj-art-d97b6fca9dba4aa68e797f99ff2ae99e2025-02-05T07:39:34ZengWorld Scientific PublishingJournal of Clinical Rheumatology and Immunology2661-34172661-34252024-12-012402788310.1142/S2661341724720039A Man with Rapidly Progressive Limb GangreneAda Wing Tung Leung0Virginia Weng Nga Lao1Department of Medicine and Geriatrics, Kwong Wah Hospital, Hong Kong SAR, ChinaDepartment of Medicine and Geriatrics, Kwong Wah Hospital, Hong Kong SAR, ChinaAntiphospholipid syndrome (APS) and polyarteritis nodosa (PAN) are two distinct, but potentially overlapping, autoimmune disorders that are characterized by vascular morbidities. We present a case of probable APS that manifested as rapidly progressive peripheral gangrene with a positive test for lupus anticoagulant (LAC), alongside with angiographic evidence of suspected renal and hepatic artery aneurysms commonly associated with PAN, but also the presence of diffuse thrombosis over the distal arterial branches in the four limbs. Through this case, we aim to review the overlapping features and potential interplay between APS and PAN, highlighting the necessary considerations for optimizing management to salvage the ongoing limb ischemia.https://www.worldscientific.com/doi/10.1142/S2661341724720039Antiphospholipid SyndromePolyarteritis NodosaPeripheral Gangrene
spellingShingle Ada Wing Tung Leung
Virginia Weng Nga Lao
A Man with Rapidly Progressive Limb Gangrene
Journal of Clinical Rheumatology and Immunology
Antiphospholipid Syndrome
Polyarteritis Nodosa
Peripheral Gangrene
title A Man with Rapidly Progressive Limb Gangrene
title_full A Man with Rapidly Progressive Limb Gangrene
title_fullStr A Man with Rapidly Progressive Limb Gangrene
title_full_unstemmed A Man with Rapidly Progressive Limb Gangrene
title_short A Man with Rapidly Progressive Limb Gangrene
title_sort man with rapidly progressive limb gangrene
topic Antiphospholipid Syndrome
Polyarteritis Nodosa
Peripheral Gangrene
url https://www.worldscientific.com/doi/10.1142/S2661341724720039
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