A Rare Case of Neuroendocrine Tumor Presenting as Isolated Scalp Swelling With Paroxysmal Symptoms

一例罕见的神经内分泌肿瘤病例,表现为孤立性头皮肿胀伴阵发性症状

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Abstract

We report a 36-year-old male with a nine-year history of recurrent left frontal scalp swelling following minor trauma, associated with local warmth, sweating, and a syncopal episode during fine-needle aspiration cytology (FNAC). Histopathology confirmed grade 2 neuroendocrine tumor (NET) with a Ki-67 index of 8-10%. 68Ga-DOTANOC positron emission tomography and computed tomography (PET-CT) showed no evidence of residual, recurrent, or primary somatostatin receptor-expressing disease, confirming this as a rare case of isolated scalp NET without an identifiable primary source. This is, to our knowledge, the first reported case of its kind. The patient's syncope post-FNAC highlights the risk of carcinoid-like crisis from lesion manipulation. This case underscores the importance of a high index of suspicion, thorough immunohistochemical workup, and consideration of peri-procedural octreotide prophylaxis.

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