Pelvic extramedullary hematopoiesis with life-threatening hemorrhage: a case report

We report the case of a 44-year-old woman with β-thalassemia major who was found to have a pelvic fat-containing mass incidentally on imaging. A diagnostic laparotomy revealed a highly vascular mass. Complete resection was not feasible due to significant hemorrhage, necessitating postoperative embolization for hemostasis. Histopathological examination confirmed the diagnosis of extramedullary hematopoiesis. Postoperatively, the patient developed severe anemia, requiring frequent transfusions. To reduce transfusion dependency, splenic artery embolization was performed. CONCLUSION: This case underscores the rare presentation of extramedullary hematopoiesis as a pelvic mass. Accurate diagnosis is critical, as surgical removal can result in severe hemorrhage and worsening anemia. Splenic artery embolization provides a valuable therapeutic approach to managing transfusion burden in such cases.

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Publication Details

Journal
International Journal of Emergency Medicine
Published
2025-02-24
DOI
https://doi.org/10.1186/s12245-025-00834-2
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
Type
article
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article

Pelvic extramedullary hematopoiesis with life-threatening hemorrhage: a case report

Mahdi Aljawad, Ali Hassan, Zainab Habbash, Sawsan Kadhem et al.
International Journal of Emergency Medicine
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

Pelvic extramedullary hematopoiesis with life-threatening hemorrhage: a case report

Mahdi Aljawad, Ali Hassan, Zainab Habbash, Sawsan Kadhem, Nawra Mujbel
article en

Abstract

We report the case of a 44-year-old woman with β-thalassemia major who was found to have a pelvic fat-containing mass incidentally on imaging. A diagnostic laparotomy revealed a highly vascular mass. Complete resection was not feasible due to significant hemorrhage, necessitating postoperative embolization for hemostasis. Histopathological examination confirmed the diagnosis of extramedullary hematopoiesis. Postoperatively, the patient developed severe anemia, requiring frequent transfusions. To reduce transfusion dependency, splenic artery embolization was performed. CONCLUSION: This case underscores the rare presentation of extramedullary hematopoiesis as a pelvic mass. Accurate diagnosis is critical, as surgical removal can result in severe hemorrhage and worsening anemia. Splenic artery embolization provides a valuable therapeutic approach to managing transfusion burden in such cases.

International Journal of Emergency MedicineVol. 18(1)
Salmaniya Medical Complex (BH), Maternity and Children's Hospital (SA)
Gender equality, Zero hunger
Openalex Percentile: Top 95%
Myeloproliferative Neoplasms: Diagnosis and Treatment
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