# Adrenal hematopoiesis in a pediatric patient with spherocytosis: A case report and literature review

**Authors:** Rawa Bapir, Ismaeel Aghaways, Sharaza Qadir Omer, Rezheen J. Rashid, Shaho F. Ahmed, Hadeel Adnan Yasseen, Hardi M. Dhahir, Honar O. Kareem, Dilan S. Hiwa, Berun A. Abdalla, Fahmi H. Kakamad

PMC · DOI: 10.1016/j.radcr.2025.04.039 · Radiology Case Reports · 2025-05-07

## TL;DR

A child with hereditary spherocytosis had a rare adrenal gland hematopoietic mass, highlighting the need for better preoperative diagnosis to avoid unnecessary surgery.

## Contribution

This case report adds to the limited literature on adrenal extramedullary hematopoiesis in children, particularly those with hereditary spherocytosis.

## Key findings

- Adrenal extramedullary hematopoiesis was confirmed histopathologically in an 11-year-old with hereditary spherocytosis.
- Approximately 75% of adrenal EMH cases occur in the right adrenal gland.
- Conservative treatment may be viable, but most cases still undergo adrenalectomy.

## Abstract

Extramedullary hematopoiesis (EMH) is extremely rare in the adrenal glands, especially in children. Because this is an underrecognized condition, the vast majority of cases are diagnosed only after adrenalectomy. An 11-year-old female with hereditary spherocytosis presented with dull right hypochondrial pain. Ultrasonography showed chronic calculous cholecystitis, and splenomegaly. A computed tomography revealed a 4 × 1.7 cm mass in the right adrenal gland with no fat content. Laparoscopic cholecystectomy with adrenalectomy was done. Histopathological examination of the adrenal mass revealed hematopoietic precursors demonstrating megakaryocytes, admixed myeloid precursors, and erythroid precursors without adipose tissue. Nearly 30 cases of adrenal EMH have been documented in the literature. Despite being a benign condition and most of the cases diagnosed incidentally, adrenalectomy was done for the majority of patients even though conservative treatment has shown good results in several case reports. Approximately 75% of cases occurred in the right adrenal gland, with bilateral and left side constituting 12.5% each. Patients with hereditary spherocytosis may present with an adrenal mass due to EMH, even in pediatric age groups. In patients with known hematologic diseases, preoperative diagnosis through functional imaging or biopsy may prevent the need for surgical intervention.

## Linked entities

- **Diseases:** hereditary spherocytosis (MONDO:0019350)

## Full-text entities

- **Diseases:** EMH (MESH:C536227), spherocytosis (MESH:C567159), hematologic diseases (MESH:D006402), hypochondrial pain (MESH:D010146), hereditary spherocytosis (MESH:D013103), splenomegaly (MESH:D013163), adrenal mass (MESH:C536030), chronic calculous cholecystitis (MESH:D002764)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12134484/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC12134484/full.md

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Source: https://tomesphere.com/paper/PMC12134484