Elhadd Tarik, Ibrahim Shahd I, Abdelmahmuod Elabbass, Webb Susan M
Pituitary Clinic, Endocrine Section, Department of Medicine, Hamad General Hospital, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.
Department of Medicine, Univ Autonoma Barcelona, Research Center for Pituitary Diseases, Institut de Recerca Sant Pau (IIB-Sant Pau) and CIBERER Unit 747, ISCIII, Department of Endocrinology, Hospital S Pau, Barcelona 08025, Spain.
JCEM Case Rep. 2025 Apr 18;3(6):luaf075. doi: 10.1210/jcemcr/luaf075. eCollection 2025 Jun.
A 62-year-old Sudanese female was diagnosed with a nonfunctioning pituitary adenoma in 2006. Despite undergoing 3 transsphenoidal surgeries and radiotherapy, her tumor persisted, causing debilitating symptoms, including headaches and visual defects. As a last resort, she was treated with pasireotide, a second-generation somatostatin analog with a broader receptor affinity than first-generation drugs. Over 6 months, the tumor mass was stabilized, and her symptoms, including headaches, disappeared. This case demonstrates a potential new therapeutic possibility for treating resistant pituitary adenoma with pasireotide, offering hope for patients when traditional treatments fail.
一名62岁的苏丹女性于2006年被诊断为无功能垂体腺瘤。尽管接受了3次经蝶窦手术和放射治疗,她的肿瘤仍持续存在,导致了使人衰弱的症状,包括头痛和视力缺陷。作为最后的手段,她接受了帕瑞肽治疗,这是一种第二代生长抑素类似物,与第一代药物相比具有更广泛的受体亲和力。在6个月的时间里,肿瘤体积稳定下来,她的症状,包括头痛,都消失了。该病例证明了用帕瑞肽治疗耐药垂体腺瘤的一种潜在新治疗可能性,为传统治疗失败的患者带来了希望。