Spontaneous splenic rupture from indeterminate dendritic cell proliferation: a case report

Author:

Iqbal Shaikh B1ORCID,Chittal Abhinandan R1ORCID,Rao Shiavax J1ORCID,Lakra Pallavi1ORCID,Bhansali Deepty2,Pyrgos George3

Affiliation:

1. Department of Medicine , MedStar Health Internal Medicine Residency Program, Baltimore, MD, USA

2. Clinical and Laboratory Pathology , Anatomic Pathology, MedStar Health, Baltimore, MD, USA

3. Pulmonology and Critical Care Medicine , MedStar Franklin Square Medical Center, Baltimore, MD, USA

Abstract

Abstract Spontaneous splenic rupture is a rare and life-threatening phenomenon, usually associated with an underlying infectious, inflammatory, hematological, neoplastic or rheumatologic condition. Indeterminate cell tumor is a rare neoplastic dendritic cell disorder that is poorly understood but shares immunophenotypic markers for Langerhans cells without Birbeck granules. A 73-year-old man presented with upper abdominal pain after an unwitnessed fall. Computed tomography angiography showed splenomegaly and a large ruptured splenic subcapsular hematoma. Intraoperative findings from an emergency laparotomy revealed a large hemoperitoneum and a ruptured spleen. Microscopic sections identified numerous, mostly poorly formed, small nodules classified as a proliferation of indeterminate dendritic cell tumors.

Publisher

Oxford University Press (OUP)

Subject

Surgery

Reference7 articles.

1. Spontaneous splenic rupture: a rare first presentation of diffuse large B cell lymphoma;Dunphy;BMJ Case Rep,2019

2. Myelodysplastic Syndromes

3. Indeterminate cell tumor of the spleen;Chen;Hum Pathol,2012

4. Laparoscopic splenectomy for spontaneous rupture of the spleen;Thapar;J Min Access Surg,2016

5. Spontaneous splenic rupture—an uncommon complication of chronic myelomonocytic leukemia;Abbasi;Leukemia Res Rep,2020

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