Article Text

47 A case of primary gastric melanoma: no light at the end of the tunnel
  1. GM Callaghan,
  2. FC Kelleher,
  3. PF Ridgway,
  4. BM Ryan
  1. Department of Gastroenterology, Oncology, Surgery, Adelaide and Meath Hospital, Tallaght and Trinity College, Dublin, Ireland


Background Malignant melanoma of the gastrointestinal tract is usually a metastasis from a cutaneous source. Primary gastric melanoma is an extremely rare clinical entity, with only 14 reported cases worldwide. It is often advanced at time of diagnosis and is associated with a poor outcome.

Aim To describe a case of primary gastric melanoma.

Method A 76 year old gentleman, presented with a one month history of fatigue and exertional dyspnoea. Laboratory investigations indicated an anaemia, with a haemoglobin level of 11.0 g/dL. Subsequent gastroscopy visualised a large, atypical, crater-like ulcerated lesion distal to the cardia in the proximal stomach.

Results Provisional histology was suggestive of a poorly differentiated adenocarcinoma but subsequent cyto-morphology and immunophenotyping were consistent with melanoma, with positive S100 protein, HMB45 and Melan A. Further molecular genetic testing revealed a V600R mutation in the BRAF gene, which is the first primary gastric melanoma with this mutation to be reported in the literature. Given the rarity of the findings, an extensive secondary work-up was undertaken, which concluded the diagnosis primary gastric melanoma.

Conclusions Primary gastric melanoma is a rare disease that can present similarly to other upper gastrointesinal lesions, with weight loss, abdominal pain, malena, and anaemia. Given its rarity, the pathogenesis is poorly understood. Lesions are often endoscopically atypical. Important points to note would include the absence of a primary lesion, as supported by a full skin examination and PET-CT findings, which can help to delineate the limitation to the stomach, thus helping to inform subsequent management.

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