Role of Immunohistochemistry in a Rare Case of Undifferentiated Soft Tissue Sarcoma with Cytohistopathological Correlation

Soft tissue sarcomas (STS) constitute a rare subset of malignancies, posing diagnostic challenges due to their varied clinical and histopathological presentations.This case report describes a young adult female who presented with a rapidly growing thigh mass initially misinterpreted as chronic hematoma on ultrasound examination.Subsequent cytological and histopathological correlation revealed features consistent with high-grade sarcoma, necessitating further characterization through immunohistochemistry (IHC).The tumour, displaying spindle cells with pleomorphic nuclei Case Reportand abundant giant cells, posed a differential diagnosis, including pleomorphic leiomyosarcoma, liposarcoma, rhabdomyosarcoma, and malignant melanoma.Immunohistochemical examination was pivotal, confirming strong Vimentin positivity and a 30% Ki67 proliferation index while ruling out CDK4, Myogenin, MDM2, S100, SMA, and CD34 markers.This case underscores the critical role of IHC in accurate diagnosis and prognosis of challenging STS cases, advocating for a multidisciplinary approach to optimize patient management.

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Publication Details

Journal
Asian Journal of Case Reports in Surgery
Published
2025-08-08
DOI
https://doi.org/10.9734/ajcrs/2025/v8i2673
Primary Topic
Sarcoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
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article

Role of Immunohistochemistry in a Rare Case of Undifferentiated Soft Tissue Sarcoma with Cytohistopathological Correlation

Manjunath S Kotennavar, Karine Jacob, K Mamatha, Satish Arakeri
Asian Journal of Case Reports in Surgery
Sarcoma Diagnosis and Treatment
article

Role of Immunohistochemistry in a Rare Case of Undifferentiated Soft Tissue Sarcoma with Cytohistopathological Correlation

Manjunath S Kotennavar, Karine Jacob, K Mamatha, Satish Arakeri
article en

Abstract

Soft tissue sarcomas (STS) constitute a rare subset of malignancies, posing diagnostic challenges due to their varied clinical and histopathological presentations.This case report describes a young adult female who presented with a rapidly growing thigh mass initially misinterpreted as chronic hematoma on ultrasound examination.Subsequent cytological and histopathological correlation revealed features consistent with high-grade sarcoma, necessitating further characterization through immunohistochemistry (IHC).The tumour, displaying spindle cells with pleomorphic nuclei Case Reportand abundant giant cells, posed a differential diagnosis, including pleomorphic leiomyosarcoma, liposarcoma, rhabdomyosarcoma, and malignant melanoma.Immunohistochemical examination was pivotal, confirming strong Vimentin positivity and a 30% Ki67 proliferation index while ruling out CDK4, Myogenin, MDM2, S100, SMA, and CD34 markers.This case underscores the critical role of IHC in accurate diagnosis and prognosis of challenging STS cases, advocating for a multidisciplinary approach to optimize patient management.

Asian Journal of Case Reports in SurgeryVol. 8(2)
Shri BM Patil Medical College (IN)
Zero hunger
Openalex Percentile: Top 69%
Sarcoma Diagnosis and Treatment
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