An unusual presentation of primary oesophagal melanoma in an elderly male: a case report

Authors

  • Deepika Gupta Pathology Department, AIIMS Gorakhpur, Uttar Pradesh, India
  • Priyanka Srivastava Pathology Department, AIIMS Gorakhpur, Uttar Pradesh, India
  • Saurabh Kedia Gastroenterology Department, AIIMS Gorakhpur, Uttar Pradesh, India
  • Shashank Shekhar Radiotherapy Department, AIIMS Gorakhpur, Uttar Pradesh, India
  • Vikas Srivastava Pathology Department, AIIMS Gorakhpur, Uttar Pradesh, India

DOI:

https://doi.org/10.18203/2320-6012.ijrms20263559

Keywords:

Primary oesophagal melanoma, Gastrointestinal bleeding, Oesophagal mass, Elderly patient, Thoracic

Abstract

Primary malignant melanoma of the oesophagus (PMME) is a very rare and highly aggressive neoplasm, representing <0.2% of all oesophageal carcinomas. Malignant melanoma usually occurs in the skin but can sometimes arise from other non-cutaneous locations, such as mucosa, uvea, upper respiratory tract, gastrointestinal tract, and genitourinary tract. In particular, primary oesophageal melanoma is an extremely rare condition that is associated with a bad prognosis because of the aggressive nature of this tumour and late diagnosis. We present a rare case of an 85-year-old patient who had complaints of per rectal bleeding, vomiting, and shortness of breath. Physical and endoscopic examination found an oesophageal tumour. Histologic examination showed changes consistent with a malignant melanoma. PMME was diagnosed on the basis of the presence of typical histomorphological and immunohistological changes. Being extremely rare, PMME is a difficult disease for diagnosis and should be included in the differential diagnoses of melanomas of the oesophagus.

 

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Published

2026-09-29

How to Cite

Gupta, D., Srivastava, P., Kedia, S., Shekhar, S., & Srivastava, V. (2026). An unusual presentation of primary oesophagal melanoma in an elderly male: a case report . International Journal of Research in Medical Sciences, 14(10), 4818–4820. https://doi.org/10.18203/2320-6012.ijrms20263559

Issue

Section

Case Reports