Department of Surgery, University of Calabar Teaching Hospital, Calabar, Nigeria.
Department of Haematology, 108337University of Calabar Teaching Hospital, University of Calabar Teaching Hospital, Calabar, Nigeria.
J Int Med Res. 2021 Dec;49(12):3000605211058860. doi: 10.1177/03000605211058860.
Osteochondromas are common in the long bones and relatively rare in the head and neck regions. We herein report a case of a solitary temporal bone osteochondroma associated with a functional pituitary adenoma hypersecreting prolactin. The patient was a 48-year-old man with progressive, painless temporal swelling associated with gradual visual loss, gynaecomastia, erectile dysfunction, and loss of libido. A brain computed tomography scan with bone windows showed right temporal sessile bony expansion and a pituitary tumour. A pituitary function test revealed hyperprolactinaemia. His symptoms resolved with medical management, and excisional biopsy of the temporal tumour confirmed an osteochondroma. To the best of our knowledge, this is the first reported case of a solitary temporal bone osteochondroma with a functional pituitary adenoma hypersecreting prolactin.
骨软骨瘤常见于长骨,而在头颈部则相对少见。我们在此报告一例孤立性颞骨骨软骨瘤,其与分泌催乳素的功能性垂体腺瘤相关。患者为 48 岁男性,表现为进行性、无痛性颞部肿胀,伴逐渐出现的视力下降、男性乳房发育、勃起功能障碍和性欲减退。头颅 CT 扫描加骨窗显示右侧颞部附壁性骨膨胀和垂体瘤。垂体功能检查显示催乳素升高。他的症状经药物治疗后缓解,颞部肿瘤的切除活检证实为骨软骨瘤。据我们所知,这是首例报道的孤立性颞骨骨软骨瘤伴分泌催乳素的功能性垂体腺瘤。