Department of Rheumatology and General Internal Medicine, NHO National Nagasaki Medical Center, Kubara 2-1001-1 Omura, Nagasaki 856-8562, Japan.
Rheumatol Int. 2013 Jan;33(1):215-8. doi: 10.1007/s00296-010-1535-x. Epub 2010 Jun 1.
A case of apoplectic lymphocytic hypophysitis complicated by polymyalgia rheumatica (PMA) is described. A 72-year-old man was admitted to our hospital due to severe headache. Two months prior to admission, the patients had exhibited recent-onset stiffness and myalgia of shoulder and pelvic girdle that was compatible with PMR. Magnetic resonance imaging revealed a mass lesion in the pituitary fossa with focal hemorrhage. Endocrinologic studies demonstrated hypopituitarism. The headache and myalgia were improving with corticosteroid treatment; however, a trans-sphenoidal surgery was performed due to visual field loss. A white-colored mass was resected, and histologic examination showed diffuse infiltration of lymphocytes and plasma cells consistent with lymphocytic hypophysitis. Post-operatively, the headache and visual field loss resolved completely. This is the first documented case of apoplectic lymphocytic hypophysitis complicating PMR, and a possible mechanism for this rare association was discussed.
现报道 1 例伴发巨细胞动脉炎(polymyalgia rheumatica,PMA)的出血性淋巴细胞性垂体炎病例。1 名 72 岁男性因严重头痛而被收入我院。入院前 2 个月,患者出现突发性肩部和骨盆带僵硬和肌痛,符合巨细胞动脉炎的表现。磁共振成像显示垂体窝内有块状病变伴局灶性出血。内分泌研究表明存在垂体功能减退。头痛和肌痛在皮质类固醇治疗后有所改善;然而,由于视野丧失,进行了经蝶窦手术。切除了白色块状物,组织学检查显示弥漫性淋巴细胞和浆细胞浸润,符合淋巴细胞性垂体炎。术后,头痛和视野丧失完全缓解。这是首例出血性淋巴细胞性垂体炎伴发巨细胞动脉炎的病例报道,并讨论了这种罕见关联的可能机制。