A rare case of adolescent Histiocytic Sarcoma

Histiocytic sarcoma is a rare haematopoietic malignancy with an aggressive nature and poor prognosis. It occurs infrequently in children and adolescents, with only a few cases reported worldwide.A well 14-year-old male patient presented with a slow-growing mass on his right lateral malleolus. Imaging suggested a benign tumour and an excision biopsy was performed. Morphological examination raised suspicion for a histiocytic neoplasm, which was confirmed by immunohistochemistry (CD68 and CD45 positive, CD1a, CD30 and ALK1 negative). Because of the tumour’s rarity, it was sent for an international confirmatory pathological review.Contribution: Our patient underwent a wide local resection followed by radiotherapy (50 Gy). No adjuvant chemotherapy was prescribed, and he has remained in remission 2 years following his diagnosis.

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Publication Details

Journal
South African Journal of Oncology
Published
2025-08-22
DOI
https://doi.org/10.4102/sajo.v9i0.324
Citations
1
Primary Topic
Histiocytic Disorders and Treatments
Type
article
Field-Weighted Citation Impact
1.16
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article

A rare case of adolescent Histiocytic Sarcoma

Duvern Ramiah, Nadia Beringer, Simon Nayler, Kate G. Bennett et al.
1 citations
South African Journal of Oncology
Histiocytic Disorders and Treatments
1.16
article

A rare case of adolescent Histiocytic Sarcoma

Duvern Ramiah, Nadia Beringer, Simon Nayler, Kate G. Bennett, Owen Terreblanche, Jacques du Toit, Himal Sooka, Doron Frantzen
article en
1 citations

Abstract

Histiocytic sarcoma is a rare haematopoietic malignancy with an aggressive nature and poor prognosis. It occurs infrequently in children and adolescents, with only a few cases reported worldwide.A well 14-year-old male patient presented with a slow-growing mass on his right lateral malleolus. Imaging suggested a benign tumour and an excision biopsy was performed. Morphological examination raised suspicion for a histiocytic neoplasm, which was confirmed by immunohistochemistry (CD68 and CD45 positive, CD1a, CD30 and ALK1 negative). Because of the tumour’s rarity, it was sent for an international confirmatory pathological review.Contribution: Our patient underwent a wide local resection followed by radiotherapy (50 Gy). No adjuvant chemotherapy was prescribed, and he has remained in remission 2 years following his diagnosis.

South African Journal of OncologyVol. 9
Wits University Donald Gordon Medical Centre (ZA)
Openalex Percentile: Top 19%
Histiocytic Disorders and Treatments
1.16
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A rare case of adolescent Histiocytic Sarcoma — Duvern Ramiah, Nadia Beringer, et al. · South African Journal of Oncology (2025) | TGRS Research Map | TGRS