S6258 A Rare Presentation of Merkel Cell Carcinoma With Gastric Metastasis

Introduction: Merkel cell carcinoma (MCC) is a rare and aggressive neoplasm of the skin. MCC impacts approximately 0.7 per 100,000 individuals each year, and the incidence is rising. Notably age, male gender, exposure to ultraviolet light, and immunosuppression are risk factors. MCC typically involves the head, neck, and extremities; less than 1% of cases involve gastric metastasis. In the United States, the 5-year survival rate for stage IV MCC is poor at 14%. Given the rarity of this disease, guidelines on the management for gastrointestinal (GI) involvement are limited. Thus, we present a case of MCC with gastric metastasis and performed a literature review of cases over the past decade to further enhance our understanding of this disease. Case Description/Methods: Herein, we present a case of a 77-year-old man with prior history of MCC who presented with acute anemia and melena. Physical exam revealed a fungating left neck mass. Labs showed low hemoglobin at 6.3 gm/dL. Upper endoscopy showed a large fungating mass in the gastric body; pathology showed MCC. The patient declined further surgical management of the gastric mass. He opted for adjuvant palliative radiation and chemotherapy. Discussion: Based on current predictions that around 3200 individuals will be diagnosed with MCC each year in the United States alone, this further gives impetus for the need for effective diagnostic and treatment modalities given the highly aggressive character of this disease. To our knowledge, there have been approximately 30 cases of MCC with gastric metastasis reported to date. Our case report adds to the growing body of evidence over the past decade that MCC with gastric involvement continues to have poor prognosis. Most patients with gastric metastases present with melena and anemia (9 of 12 cases). Endoscopy showed a range of mucosal lesions across cases. All 11 cases were cytokeratin-20 positive on histology (1 case did not mention whether CK20 staining was done). Non-surgical management was pursued for most patients due to poor performance status (n = 6); 5 patients underwent gastric resection; and 1 patient underwent embolization of tumor arteries. Chemotherapy was administered to 4 patients. Immunotherapy (with gastric resection) was used for 2 patients. Currently, there is no standardized treatment for MCC with gastric metastases. Given its aggressive nature, high clinical suspicion and close surveillance are necessary to improve outcomes.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001153492.60717.1e
Primary Topic
Polyomavirus and related diseases
Type
article
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article

S6258 A Rare Presentation of Merkel Cell Carcinoma With Gastric Metastasis

The American Journal of Gastroenterology
Polyomavirus and related diseases
article

S6258 A Rare Presentation of Merkel Cell Carcinoma With Gastric Metastasis

article en

Abstract

Introduction: Merkel cell carcinoma (MCC) is a rare and aggressive neoplasm of the skin. MCC impacts approximately 0.7 per 100,000 individuals each year, and the incidence is rising. Notably age, male gender, exposure to ultraviolet light, and immunosuppression are risk factors. MCC typically involves the head, neck, and extremities; less than 1% of cases involve gastric metastasis. In the United States, the 5-year survival rate for stage IV MCC is poor at 14%. Given the rarity of this disease, guidelines on the management for gastrointestinal (GI) involvement are limited. Thus, we present a case of MCC with gastric metastasis and performed a literature review of cases over the past decade to further enhance our understanding of this disease. Case Description/Methods: Herein, we present a case of a 77-year-old man with prior history of MCC who presented with acute anemia and melena. Physical exam revealed a fungating left neck mass. Labs showed low hemoglobin at 6.3 gm/dL. Upper endoscopy showed a large fungating mass in the gastric body; pathology showed MCC. The patient declined further surgical management of the gastric mass. He opted for adjuvant palliative radiation and chemotherapy. Discussion: Based on current predictions that around 3200 individuals will be diagnosed with MCC each year in the United States alone, this further gives impetus for the need for effective diagnostic and treatment modalities given the highly aggressive character of this disease. To our knowledge, there have been approximately 30 cases of MCC with gastric metastasis reported to date. Our case report adds to the growing body of evidence over the past decade that MCC with gastric involvement continues to have poor prognosis. Most patients with gastric metastases present with melena and anemia (9 of 12 cases). Endoscopy showed a range of mucosal lesions across cases. All 11 cases were cytokeratin-20 positive on histology (1 case did not mention whether CK20 staining was done). Non-surgical management was pursued for most patients due to poor performance status (n = 6); 5 patients underwent gastric resection; and 1 patient underwent embolization of tumor arteries. Chemotherapy was administered to 4 patients. Immunotherapy (with gastric resection) was used for 2 patients. Currently, there is no standardized treatment for MCC with gastric metastases. Given its aggressive nature, high clinical suspicion and close surveillance are necessary to improve outcomes.

The American Journal of GastroenterologyVol. 120(10S2)
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Openalex Percentile: Top 32%
Polyomavirus and related diseases
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