Immune Thrombocytopenic Purpura Secondary to Sarcoidosis.


Journal

Maedica
ISSN: 1841-9038
Titre abrégé: Maedica (Bucur)
Pays: Romania
ID NLM: 101526930

Informations de publication

Date de publication:
Mar 2022
Historique:
entrez: 23 6 2022
pubmed: 24 6 2022
medline: 24 6 2022
Statut: ppublish

Résumé

Sarcoidosis is a systemic granulomatous disease involving multiple organs with predominantly pulmonary manifestations. Severe thrombocytopenia is a relatively rare hematologic manifestation of sarcoidosis. Immune thrombocytopenia is usually characterized by excessive antibody production leading to platelet destruction. There are a few reported cases of immune thrombocytopenic purpura secondary to sarcoidosis, but the pathophysiologic mechanism remains unknown. We report the case of a 65-year-old woman who presented severe thrombocytopenia and was found to have immune thrombocytopenic purpura secondary to sarcoidosis.

Identifiants

pubmed: 35733729
doi: 10.26574/maedica.2022.17.1.234
pmc: PMC9168564
doi:

Types de publication

Editorial

Langues

eng

Pagination

234-236

Références

Sarcoidosis Vasc Diffuse Lung Dis. 2006 Oct;23(3):229-35
pubmed: 18038923
J Pediatr. 1972 Oct;81(4):758-64
pubmed: 4672589
Proc (Bayl Univ Med Cent). 2021 Sep 15;35(1):60-61
pubmed: 34970034
Medicine (Baltimore). 2011 Jul;90(4):269-278
pubmed: 21694642
Br J Haematol. 2007 Nov;139(4):605-11
pubmed: 17979946
Pneumonol Alergol Pol. 2011;79(5):371-6
pubmed: 21861263
Respir Med. 2018 May;138S:S38-S44
pubmed: 29055517
South Med J. 1992 Jul;85(7):775-8
pubmed: 1631702

Auteurs

Aisha Barlas (A)

Department of Internal Medicine, Javon Bea Hospital, Rockford, USA.

Lintu Ramachandran (L)

Department of Internal Medicine, Javon Bea Hospital, Rockford, USA.

Classifications MeSH