A Case Report: Primary Malignant Melanoma of the Jejunum
DOI:
https://doi.org/10.21276/apalm.3542Keywords:
Malignant melanoma, Primary intestinal melanoma, Jejunum, Small bowel intussusception, Gastrointestinal melanomaAbstract
Background: Malignant melanoma represents only less than 3% of all malignant tumors in the gastrointestinal (GI) tract. Differentiating primary melanomas from metastatic melanoma can be difficult.
Case Presentation: We report the case of a 60-year-old woman who presented with signs of intestinal obstruction. An USG abdomen and KUB shows intussusception small bowel, and CT imaging revealed a mass in the proximal small intestine. Emergency laparotomy was performed, which identified an intraluminal tumor in the proximal jejunum. This tumor was surgically resected, followed by end-to-end anastomosis. Histopathological and immunohistochemical analyses confirmed malignant melanoma, with tumor cells testing positive for S-100, HMB-45, and Melan-A. A comprehensive postoperative evaluation including whole-body PET-CT, dermatological, ophthalmological, and nodal assessments showed no evidence of a primary cutaneous, mucosal, ocular, or nodal lesion, nor any additional metastases. These findings supported the diagnosis of primary jejunal melanoma, an exceedingly rare condition.
Outcome: The patient recovered without complications and was referred to medical oncology. She began adjuvant immunotherapy with nivolumab. At the 6-month follow-up, she remained clinically asymptomatic, with no evidence of recurrence observed in surveillance imaging. Conclusion: In rare but significant instances of small intestinal obstruction, primary malignant melanoma of the small intestine is taken into consideration. The best results can only be obtained with early surgical intervention, a precise histological diagnosis, and prompt immunotherapy treatment.
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Copyright (c) 2025 Geethu Krishnan, Pragnesh H. Shah

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