# Case Report: Post-splenectomy bulky pelvic splenosis in an adolescent with hereditary spherocytosis

## TL;DR

A 16-year-old girl with a history of splenectomy for hereditary spherocytosis developed a pelvic mass that was diagnosed as splenosis, not cancer.

## Contribution

This case report highlights the rare complication of splenosis following splenectomy and emphasizes its importance in differential diagnosis.

## Key findings

- Pelvic splenosis was confirmed in a patient with a history of splenectomy through laparoscopy and histopathology.
- The patient remained asymptomatic, leading to conservative management instead of surgical intervention.
- The case underscores the diagnostic challenge splenosis can pose, as it may mimic malignancies.

## Abstract

Splenectomy is a well-established therapeutic approach for pediatric hematologic disorders, especially in the case of hereditary spherocytosis (HS). In addition to the commonly acknowledged short- and long-term infectious and thrombotic complications, also splenosis represents a rare but noteworthy complication of splenectomy. Splenosis is characterized by the auto-transplantation and growth of splenic tissue in ectopic locations, following trauma or splenectomy. This condition can mimic malignancies, posing diagnostic challenges. We report the case of a 16-year-old girl with HS who presented with fever, abdominal pain, and a history of laparoscopic splenectomy ten years early. Imaging revealed a vascularized pelvic mass, initially suspected to be malignant. Diagnostic laparoscopy and histopathological analysis confirmed the mass as pelvic splenosis. The patient was asymptomatic, prompting a conservative management approach with regular follow-up. This case highlights the importance of considering splenosis in differential diagnoses for pelvic masses in patients with prior splenectomy, to ensure appropriate management and avoid unnecessary interventions.