Romeo Stefano, Milione Massimo, Gatti Alessandra, Fallarino Mara, Corleto Vito, Morano Susanna, Baroni Marco Giorgio
Department of Medical Sciences, Endocrinology and Metabolism, University of Cagliari, Cagliari, Italy.
Horm Res. 2006;65(3):120-5. doi: 10.1159/000091408. Epub 2006 Feb 9.
Insulinoma is the most common pancreatic endocrine tumor, accounting for 40% of all pancreatic functional neoplasm, and is characterized by hypersecretion of insulin and hypoglycemia. Elective treatment for insulinomas is surgical enucleation. Medical therapy with diazoxide, followed by somatostatin analogues in some cases, may be necessary to treat the hypoglycemic symptoms. We report a case of a patient affected by metastatic insulinoma with severe hypoglycemia. After surgery, histopathology confirmed the presence of a malignant insulinoma with multiple metastases in the liver. Due to the persistence of hypoglycemia, the patient was started on octreotide LAR treatment, which determined a complete clinical remission with regression of the metastatic lesions in the liver after one year. Repeated CT scans 2 and 3 years after surgery confirmed the remission. To our knowledge, the complete regression of the disease in insulinomas treated with long-standing somatostatin analogue therapy has never been reported. Immunohistochemical analysis in tissue specimens showed a strong membrane immunoreactivity for somatostatin receptors type 2 (SSTR2) in both the primary nodule and the metastases. The capacity of somatostatin analogues to negatively regulate cell proliferation through indirect and direct mechanisms has been experimentally demonstrated. Furthermore, SSTR2 activation may exert pro-apoptotic effects in neoplastic cells. Thus, both mechanisms may have been responsible of the remission of the disease in this patient. This case underlies the potential impact of the treatment of pancreatic insulinomas with somatostatin analogues, and, if confirmed, the usefulness of SSTR determination in these neoplastic specimens.
胰岛素瘤是最常见的胰腺内分泌肿瘤,占所有胰腺功能性肿瘤的40%,其特征是胰岛素分泌过多和低血糖。胰岛素瘤的择期治疗是手术摘除。对于低血糖症状,可能需要先用二氮嗪进行药物治疗,某些情况下随后使用生长抑素类似物。我们报告一例患有转移性胰岛素瘤并伴有严重低血糖的患者。手术后,组织病理学证实存在恶性胰岛素瘤且肝脏有多处转移。由于低血糖持续存在,患者开始接受长效奥曲肽治疗,一年后临床完全缓解,肝脏转移病灶消退。术后2年和3年的重复CT扫描证实了缓解情况。据我们所知,长期使用生长抑素类似物治疗胰岛素瘤后疾病完全消退的情况此前从未有过报道。组织标本的免疫组化分析显示,原发结节和转移灶中生长抑素2型受体(SSTR2)均有强烈的膜免疫反应性。生长抑素类似物通过间接和直接机制对细胞增殖进行负调控的能力已在实验中得到证实。此外,SSTR2激活可能在肿瘤细胞中发挥促凋亡作用。因此,这两种机制可能都是该患者疾病缓解的原因。该病例凸显了生长抑素类似物治疗胰腺胰岛素瘤的潜在影响,若得到证实,也凸显了在这些肿瘤标本中检测SSTR的有用性。