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Case report reveals rapid disease progression in primary neuroendocrine tumor, highlighting diagnostic challenges.
Primary neuroendocrine tumors (NETs) of bone are exceedingly rare, and most osseous NETs represent metastases from an occult primary site. We report a rare case of primary NET arising from the left superior pubic ramus, presenting as progressive left inguinal swelling. An 83-year-old male presented with groin swelling, pain, and limping for 3 months. Radiographs and contrast-enhanced computed tomography demonstrated an osteolytic lesion in the left superior pubic ramus with an associated soft-tissue mass. Magnetic resonance imaging showed an aggressive marrow-replacing lesion with central necrosis, cortical destruction, soft-tissue extension, and regional lymphadenopathy, initially suggesting metastatic disease or primary bone sarcoma. Comprehensive systemic evaluation excluded an extra-osseous primary tumor. Biopsy with immunohistochemistry confirmed neuroendocrine differentiation, with a Ki–67 index consistent with World Health Organization (Grade 2). A diagnosis of primary osseous NET was established. Despite chemotherapy and radiotherapy, rapid disease progression occurred, and the patient expired, emphasizing diagnostic challenges and the importance of radiologic–pathologic correlation.
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Kaur et al. (2026) studied this question.
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