| Literature DB >> 35257302 |
Vittorio Durastante1, Antonello Conte2, Pier Paolo Brollo3, Carlo Biddau4, Michele Graziano5, Vittorio Bresadola3.
Abstract
INTRODUCTION: Merkel cell carcinoma (MCC) is an infrequent, but highly aggressive neuroendocrine neoplasm of the skin with a propensity for recurrence and metastasis. We report a rare case of gastric metastatic localization of this cancer by focusing on the diagnostic, clinical, and surgical approach to the patient. CASE REPORT: Clinical presentation begins with a peripheral lymphadenopathy whose immunohistochemical characterization identifies the lymphatic dissemination of the disease. Gradually, the patient develops a severe anaemic state which requires several blood transfusions and surgical gastric resection to remove a large bleeding lesion of the antral region. The histopathological analysis of the specimen confirms the metastatic origin from MCC, but the primitive lesion remains unknown. DISCUSSION: Since this clinical situation is very rare, we conducted a review of the literature selecting the few cases reported, in order to evaluate the current knowledge on this topic. Metastatic involvement of the stomach from Merkel cell carcinoma is a rare presentation of this disease progression with a frequent delay in formulating the correct diagnosis and in further treatment which may be life-threatening for the patient. As regards the local treatment, there is no specific guideline, and the therapeutic indication should be tailored on the specific case.Entities:
Keywords: Gastric metastasis; Gastric surgery; Immunotherapy for cancer; Merkel cell carcinoma; Neuroendocrine tumors
Year: 2022 PMID: 35257302 DOI: 10.1007/s12029-022-00817-z
Source DB: PubMed Journal: J Gastrointest Cancer