Ahmed Momin, Ardor Gokce Deniz, Hanna Helena, Alhaj Ahmed M, Nassar Aziza
Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine and Science, 4500 Pablo Road, FL 32224, USA; University of Florida, 300 Southwest 13th Street, Gainesville, FL 32611, USA.
Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine and Science, 4500 Pablo Road, FL 32224, USA.
Int J Surg Case Rep. 2023 Feb;103:107907. doi: 10.1016/j.ijscr.2023.107907. Epub 2023 Feb 3.
Gastrointestinal tract (GIT) is a common site for malignant melanoma metastasis, with small bowel being the most common. It is usually difficult to diagnose at an early stage because of the anatomical location of the disease. It is also challenging for pathologists to diagnose due to the small amount of biopsy samples. Survival rates of melanoma patients with distant metastasis are very poor.
This study presents two males, aged 67 and 69 years old, who have metastatic melanoma within the GIT. One was metastasis to the esophagus and another with metastasis to the jejunum presenting as intraluminal masses. Their clinical history and pathologic features of the metastasis are evaluated to give an insight into this disease.
Gastrointestinal melanoma is hard to detect due to its anatomical location and limited ability to biopsy. Typically, they present at an advanced stage when diagnosed. Approximately 60 % of patients with cutaneous melanoma will have GIT metastasis at the time of autopsy. The small bowel was found to have an affinity for malignant melanoma due to the expression of the CCR9 ligand, CCL25. BRAF mutations are much less observed in GIT mucosal melanomas as compared to cutaneous melanomas. Furthermore, AKAP13-NTRK3 fusion has been reported specifically in the GIT mucosal melanomas. NTRK fusions in general can be observed in metastatic melanomas and have been reported in GIT metastatic melanomas.
GIT malignant melanomas are difficult to detect due to their anatomical location, with poor prognosis, and have a unique genetic profile.
胃肠道(GIT)是恶性黑色素瘤转移的常见部位,其中小肠最为常见。由于该疾病的解剖位置,通常很难在早期进行诊断。此外,由于活检样本量少,病理学家进行诊断也具有挑战性。远处转移的黑色素瘤患者的生存率非常低。
本研究报告了两名男性,年龄分别为67岁和69岁,他们患有胃肠道转移性黑色素瘤。一名患者转移至食管,另一名患者转移至空肠,表现为腔内肿块。对他们的临床病史和转移的病理特征进行了评估,以深入了解这种疾病。
胃肠道黑色素瘤因其解剖位置和有限的活检能力而难以检测。通常,它们在诊断时已处于晚期。在尸检时,约60%的皮肤黑色素瘤患者会发生胃肠道转移。由于CCR9配体CCL25的表达,发现小肠对恶性黑色素瘤具有亲和力。与皮肤黑色素瘤相比,胃肠道黏膜黑色素瘤中BRAF突变的观察结果要少得多。此外,AKAP13-NTRK3融合已在胃肠道黏膜黑色素瘤中被特别报道。一般来说,NTRK融合可在转移性黑色素瘤中观察到,并且已在胃肠道转移性黑色素瘤中被报道。
胃肠道恶性黑色素瘤因其解剖位置难以检测,预后较差,且具有独特的基因特征。