Visceral metastases from malignant melanoma (stage M1c) confer a very poor prognosis, as documented on the most recent revised version of the TNM/AJCC staging system. Emergency surgery for intra-abdominal complications from the disease is rare. We report on our 5-year single institution experience with surgical management of metastatic melanoma to the viscera in the emergent setting. From 2009 to 2013, 14 patients with metastatic melanoma were admitted emergently due to an acute abdomen. Clinical manifestations encompassed intestinal obstruction and bleeding. Surgical procedures involved multiple enterectomies with primary anastomoses in 8 patients, and one patient underwent splenectomy, one adrenalectomy, one right colectomy, one gastric wedge resection, one gastrojejunal anastomosis, and one transanal debulking, respectively. The 30-day mortality was 7 percent. Median follow-up was 14 months. Median overall survival was 14 months. Median disease free survival was 7.5 months. One-year overall survival was 64.2 percent and 2-year overall survival was 14.2 percent. Emergency surgery for metastatic melanoma to the viscera is rare. Elective curative surgery combined with novel cytotoxic systemic therapies is under investigation in an attempt to grant survival benefit in melanoma patients with visceral disease. 1. Introduction Metastatic melanoma is an aggressive disease with dismal prognosis despite novel chemotherapeutic agents. M1c disease is defined as the presence of visceral metastases with elevated lactate dehydrogenase (LDH) level in the absence of pulmonary metastasis and carries a median survival of about 6 to 10 months [1]. Advanced melanoma can disseminate to any organ, with the commonest distant sites of metastasis being the skin, lung, and brain. In cases of visceral involvement, metastatic malignant melanoma most commonly attains the liver and the small bowel. Interestingly, up to 95 percent of patients with metastases to the gastrointestinal tract will not be identified until autopsy [1]. Intra-abdominal dissemination of melanoma can manifest itself with weight loss, vague abdominal pain, and/or anemia. In some cases, patients can present in the emergency setting with bowel intussusception, obstruction, bleeding, or perforation [2]. Although an acute abdominal symptomatology can raise the suspicion of intra-abdominal metastasis in any patient with a history of cutaneous melanoma, diagnosis is definitely made at surgery. We report on our five-year, single-center experience in emergency surgery for M1c melanoma. 2. Case Series Between 2009 and
References
[1]
A. M. Leung, D. M. Hari, and D. L. Morton, “Surgery for distant melanoma metastasis,” Cancer Journal, vol. 18, no. 2, pp. 176–184, 2012.
[2]
S. Shenoy and R. Cassim, “Metastatic melanoma to the gastrointestinal tract: role of surgery as palliative treatment,” The West Virginia Medical Journal, vol. 109, no. 1, pp. 30–33, 2013.
[3]
C. M. Balch, A. N. Houghton, A. J. Sober, et al., Eds., Cutaneous Melanoma, Quality Medical Publishing, St. Louis, Mo, USA, 2009.
[4]
M. Maio, P. Ascierto, A. Testori, et al., “The cost of unresectable stage III or stage IV melanoma in Italy,” Journal of Experimental & Clinical Cancer Research, vol. 31, p. 91, 2012.
[5]
C. Bedane, M.-T. Leccia, B. Sassolas, B. Bregman, and C. Lebbé, “Treatment patterns and outcomes in patients with advanced melanoma in France,” Current Medical Research and Opinion, vol. 29, no. 10, pp. 1297–1305, 2013.
[6]
K. P. Wevers and H. J. Hoekstra, “Stage IV melanoma: completely resectable patients are scarce,” Annals of Surgical Oncology, vol. 20, no. 7, pp. 2352–2356, 2013.
[7]
T. C. Chua, A. Saxena, and D. L. Morris, “Surgical metastasectomy in AJCC stage IV M1c melanoma patients with gastrointestinal and liver metastases,” Annals of the Academy of Medicine, vol. 39, no. 8, pp. 634–639, 2010.
[8]
S. R. Martinez and S. E. Young, “A rational surgical approach to the treatment of distant melanoma metastases,” Cancer Treatment Reviews, vol. 34, no. 7, pp. 614–620, 2008.
[9]
T. Tomov, R. Siegel, and A. Bembenek, “Long-term survival in stage IV melanoma after repetitive surgical therapy,” Onkologie, vol. 31, no. 5, pp. 259–261, 2008.
[10]
P. J. Mosca, E. Teicher, S. P. Nair, and B. A. Pockaj, “Can surgeons improve survival in stage IV melanoma?” Journal of Surgical Oncology, vol. 97, no. 5, pp. 462–468, 2008.
[11]
S. E. Young, S. R. Martinez, and R. Essner, “The role of surgery in treatment of stage IV melanoma,” Journal of Surgical Oncology, vol. 94, no. 4, pp. 344–351, 2006.
[12]
N. Wasif, S. P. Bagaria, P. Ray, and D. L. Morton, “Does metastasectomy improve survival in patients with stage IV melanoma? A cancer registry analysis of outcomes,” Journal of Surgical Oncology, vol. 104, no. 2, pp. 111–115, 2011.
[13]
C. Vallicelli, F. Coccolini, F. Catena, et al., “Small bowel emergency surgery: literature's review,” World Journal of Emergency Surgery, vol. 6, article 1, 2011.
[14]
M. C. Wyers, “Acute mesenteric ischemia: diagnostic approach and surgical treatment,” Seminars in Vascular Surgery, vol. 23, no. 1, pp. 9–20, 2010.
[15]
K. Woods, E. Williams, W. Melvin, and K. Sharp, “Acquired jejunoileal diverticulosis and its complications: a review of the literature,” The American Surgeon, vol. 74, no. 9, pp. 849–854, 2008.
[16]
F. Catena, L. Ansaloni, F. Gazzotti, et al., “Small bowel tumours in emergency surgery: specificity of clinical presentation,” ANZ Journal of Surgery, vol. 75, no. 11, pp. 997–999, 2005.
[17]
S. B. Williams, J. Greenspon, H. A. Young, and B. A. Orkin, “Small bowel obstruction: conservative vs. surgical management,” Diseases of the Colon & Rectum, vol. 48, no. 6, pp. 1140–1146, 2005.
[18]
B. Szynglarewicz, M. Ekiert, J. Forgacz, A. Halon, R. Skalik, and R. Matkowski, “The role of surgery in the treatment of colorectal metastases from primary skin melanoma,” Colorectal Disease, vol. 14, no. 6, pp. e305–e311, 2012.
[19]
B. Shpitz, Z. Kaufman, A. Gildor, and A. Dinbar, “Metastatic malignant melanoma of the small bowel as a surgical emergency,” Harefuah, vol. 119, no. 11, pp. 364–365, 1990.
[20]
A. Giacobbe, D. Facciorusso, G. Modola, and A. Andriulli, “Metastatic melanoma: endoscopy as aid to earlier in vivo diagnosis of gastrointestinal involvement. A case report,” Minerva Gastroenterologica e Dietologica, vol. 42, no. 3, pp. 169–171, 1996.
[21]
R. H. Richter, B. Reingruber, C. Grüneis, A. Altendorf-Hofmann, and H. Rupprecht, “Spontaneous splenic rupture in metastatic malignant melanoma,” Zentralblatt fur Chirurgie, vol. 126, no. 8, pp. 630–631, 2001.
[22]
E. Castellani, P. Covarelli, C. Boselli et al., “Spontaneous splenic rupture in patient with metastatic melanoma treated with vemurafenib,” World Journal of Surgical Oncology, vol. 10, article 155, 2012.
[23]
T. Frieling, J. Heise, and S. W. Wassilew, “Multiple colon ulcerations, perforation and death during treatment of malignant melanoma with sorafenib,” Deutsche medizinische Wochenschrift, vol. 134, no. 28-29, pp. 1464–1466, 2009.
[24]
M. Wantz, F. Antonicelli, C. Derancourt, P. Bernard, M. F. Avril, and F. Grange, “Long-term survival and spontaneous tumor regression in stage IV melanoma: possible role of adrenalectomy and massive tumor antigen release,” Annales de Dermatologie et de Venereologie, vol. 137, pp. 464–467, 2010.
[25]
T. Namikawa and K. Hanazaki, “Clinicopathological features and treatment outcomes of metastatic tumors in the stomach,” Surgery Today, vol. 44, no. 8, pp. 1392–1399, 2014.
[26]
N. Mourra, A. Jouret-Mourin, T. Lazure, et al., “Metastatic tumors to the colon and rectum: a multi-institutional study,” Archives of Pathology & Laboratory Medicine, vol. 136, no. 11, pp. 1397–1401, 2012.
[27]
M. C. Fox, C. D. Lao, J. L. Schwartz, M. L. Frohm, C. K. Bichakjian, and T. M. Johnson, “Management options for metastatic melanoma in the era of novel therapies: a primer for the practicing dermatologist: part II: management of stage IV disease,” Journal of the American Academy of Dermatology, vol. 68, no. 1, pp. 13.e1–13.e13, 2013.