Key result
Diaphragmatic spindle cell rhabdomyosarcoma presents with progressive breathlessness and pleuritic chest pain in a 41-year-old man.
Why the study?
Rhabdomyosarcoma is an uncommon malignant soft-tissue tumor, with diaphragmatic spindle cell rhabdomyosarcoma being extremely rare in adults.
This case report highlights an extremely rare presentation of diaphragmatic spindle cell rhabdomyosarcoma in an adult, demonstrating the necessity of multimodality imaging and biopsy for accurate diagnosis.
Underscores need for multimodality imaging and biopsy in atypical breathlessness; hypothesis-generating for rare adult diaphragmatic sarcomas.
Rhabdomyosarcoma (RMS) is an uncommon malignant soft-tissue tumor, with diaphragmatic spindle cell RMS being extremely rare in adults. A 41-year-old male patient had progressive breathlessness and right-sided pleuritic chest pain. Imaging and biopsy that includes X-ray, computed tomography, magnetic resonance imaging, histopathology, and immunohistochemistry established a large thoracoabdominal spindle cell RMS. Early diagnosis, careful imaging, and combined treatment were important, and they helped increase knowledge of this unusual entity.
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Gulve et al. (2026) studied this question. Diaphragmatic spindle cell rhabdomyosarcoma with thoracoabdominal extension was diagnosed in a 41-year-old male presenting with progressive breathlessness and pleuritic chest pain.
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