A case of immune thrombocytopenic purpura secondary to endometriosis causing a pelvic haematoma

Chipwete S, Saliya Chipwete, Saliya Ellen Chipwete, Yogesh Jethava, Janice Rymer, Rymer J
BMJ case reports · 2011 · vol. 2011 , pp. bcr0920103329 · doi:10.1136/bcr.09.2010.3329 · PMID:22714615 · PMC3062346 · W2111074895
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⚙ AI-generated summary by claude@2026-06, 2026-06-12 ⓘ

A 51-year-old woman with endometriosis developed severe immune thrombocytopenic purpura and a pelvic hematoma, along with ureteral obstruction and renal failure, which resolved with immunoglobulin and steroid treatment.

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Abstract

The authors present a case of a 51-year-old woman with endometriosis who developed immune thrombocytopenic purpura. Her platelets dropped to 2×10(9)/l, and she had haemorrhage into her right endometrioma causing a large pelvic haematoma. She also had renal failure secondary to endometriosis compressing the right ureter. She was treated with immunoglobulin and steroids with subsequent recovery of platelet count and underwent ureteric stenting to prevent worsening renal function.

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Condition tags

endometriosisendometrioma

MeSH descriptors

Endometriosis Hematoma Purpura, Thrombocytopenic, Idiopathic Endometriosis Female Hematoma Humans Middle Aged Pelvis Purpura, Thrombocytopenic, Idiopathic Purpura, Thrombocytopenic, Idiopathic

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (12)

Source provenance

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