Fiebiger W, Kurtaran A, Novotny C, Kainberger F, Dekan G, Raderer M
Department of Internal Medicine I, Division of Oncology, University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Ann Hematol. 2003 Jun;82(6):374-6. doi: 10.1007/s00277-003-0625-1. Epub 2003 Apr 29.
Carcinoid tumors are relatively rare neuroendocrine malignancies with an indolent clinical behavior. The majority of cases arise within the gastrointestinal tract, but they may also be encountered in other organs such as the bronchial system. While occurrence of carcinoid tumors has been reported in association with the multiple endocrine neoplasia (MEN) type I syndrome, no clear-cut risk factors have been established for the development of these malignancies. We report the case of a 50-year-old woman who was diagnosed with a pulmonary carcinoid in 2001 after having undergone allogeneic stem cell transplantation for chronic myeloid leukemia (CML) in 1997. This is the first case report of a carcinoid tumor following allogeneic bone marrow transplantation. At the moment, however, an association with CML as well as a causative role of transplantation and intake of immunosuppressants remains speculative. Apart from highlighting the occurrence of a carcinoid in this setting, our case again underscores the importance of nuclear medicine methods, i.e., somatostatin receptor scintigraphy, in staging and follow-up of patients with carcinoid tumors.
类癌是相对罕见的神经内分泌恶性肿瘤,临床行为惰性。大多数病例发生在胃肠道,但也可见于其他器官,如支气管系统。虽然已有报道类癌的发生与I型多发性内分泌肿瘤(MEN)综合征有关,但这些恶性肿瘤发生的明确危险因素尚未确立。我们报告一例50岁女性,她于1997年因慢性粒细胞白血病(CML)接受异基因干细胞移植,2001年被诊断为肺类癌。这是首例异基因骨髓移植后发生类癌肿瘤的病例报告。然而,目前其与CML的关联以及移植和免疫抑制剂摄入的致病作用仍属推测。除了强调这种情况下类癌的发生外,我们的病例再次强调了核医学方法,即生长抑素受体闪烁扫描术,在类癌肿瘤患者分期和随访中的重要性。