Abstract

BackgroundClear cell sarcoma of soft parts is most commonly found associated with the tendons and aponeuroses of distal extremities in young adults with a peak incidence in the third decade. Location in the abdominal wall and in a child is very rare.Case presentationA nine-year-old female child presented with a swelling in the anterior abdominal wall in the suprapubic region. Fine needle aspiration revealed predominantly discrete cells with loose clustering at places. The cytoplasm was abundant, finely granular, and eosinophilic with some cells exhibiting clear vacuolated zones. No pigment was seen. The nuclei were rounded and eccentrically placed with a striking single eosinophilic macro nucleolus present in all the cells. Taking into consideration, the history, age of the patient, location of the tumor and absence of melanin pigment, a diagnosis of soft tissue sarcoma was made, the differential including Clear cell sarcoma. This was subsequently confirmed on histopathological examination and immunohistochemistryConclusionThe atypical presentation of the case made the cytological diagnosis rather challenging. Clear cell sarcoma should be considered when cytology of a soft-tissue tumor shows uncharacteristically high cellularity and relatively uniform cells with macronucleoli.

Highlights

  • cell sarcoma of the soft parts (CCS) is most commonly found associated with the tendons and aponeuroses of distal extremities in young adults with a peak incidence in the third decade [2]

  • The diagnosis of CCS on fine needle aspiration cytology requires a high degree of suspicion given its rarity of presentation and overlap of mor

  • We describe the cytological features of CCS in a child presenting in the rectus abdominis tendon, an extremely rare location

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Summary

Conclusion

Cases of CCS are uncommon below the age of ten years. The location of the tumor in the present case – the rectus abdominus tendon, is extremely rare. The tumor may simulate other soft tissue sarcomas with epithelioid morphology. The diagnostic difficulty is compounded in cases with unusual clinical presentation, though the cytological features of high cellularity with dyscohesive cells showing clearing of cytoplasm and macronucleoli often offers a substantial clue in arriving at an accurate diagnosis

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Enzinger FM
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