Kuge Atsushi, Sato Shinya, Takemura Sunao, Sakurada Kaori, Kondo Rei, Kayama Takamasa
Department of Neurosurgery, Yamagata University Faculty of Medicine, 2-2-2 Iidanishi, Yamagata City, Japan.
Surg Neurol Int. 2011 Jan 24;2:3. doi: 10.4103/2152-7806.76140.
Pituitary abscess is an extremely rare finding. The abscess may arise as a primary pituitary lesion or be associated with parasellar pathology. It is important for pituitary abscess treatments to perform early diagnosis. In this report, we describe a case of pituitary adenoma in which MRI findings changed during the follow-up period and strongly suggested progression to pituitary abscess arising from adenoma.
In a 73-year-old female, pituitary adenoma had been incidentally detected; MRI showed typical findings of pituitary adenoma, and we had followed up the pituitary lesion and clinical symptoms. Six months later, she had oculomotor nerve palsy and symptoms of hypopituitarism. Hematological examination revealed inflammation and hypopituitarism. MRI showed striking changes in the signal intensity of the pituitary lesion, and strongly suggested occurrence of sinusitis and pituitary abscess ascribed to pituitary adenoma. She was admitted and endoscopic transsphenoidal surgery was performed. The sellar floor was destroyed, and yellowish-white creamy pus was observed. A histopathological study using hematoxylin-eosin staining showed adenoma and inflammatory cells. Aerobic, anaerobic, and fungal cultures were negative. Antibiotics were administered and hormonal replacement was started. Neurological and general symptoms were improved, and postoperative MRI revealed complete evacuation of abscess and removal of tumor.
Pituitary abscess within invasive pituitary adenoma is a rare entity, and shows high mortality. Early diagnosis of pituitary abscess is very important for the prompt surgery and initiation of treatment with antibiotics. In our case, changes in MRI findings were helpful to diagnose pituitary abscess, and endoscopic transsphenoidal surgery was an optimal surgical treatment.
垂体脓肿是一种极其罕见的病症。脓肿可能作为原发性垂体病变出现,或与鞍旁病变相关。早期诊断对于垂体脓肿的治疗至关重要。在本报告中,我们描述了一例垂体腺瘤病例,其磁共振成像(MRI)表现在随访期间发生变化,强烈提示腺瘤进展为垂体脓肿。
一名73岁女性偶然发现垂体腺瘤;MRI显示垂体腺瘤的典型表现,我们对垂体病变和临床症状进行了随访。六个月后,她出现动眼神经麻痹和垂体功能减退症状。血液学检查显示有炎症和垂体功能减退。MRI显示垂体病变的信号强度有显著变化,强烈提示由垂体腺瘤引起的鼻窦炎和垂体脓肿。她入院并接受了内镜经蝶窦手术。蝶鞍底部被破坏,观察到黄白色脓性分泌物。苏木精-伊红染色的组织病理学研究显示有腺瘤和炎性细胞。需氧、厌氧和真菌培养均为阴性。给予抗生素治疗并开始激素替代治疗。神经和全身症状得到改善,术后MRI显示脓肿完全清除且肿瘤被切除。
侵袭性垂体腺瘤内的垂体脓肿是一种罕见病症,死亡率高。垂体脓肿的早期诊断对于及时手术和开始抗生素治疗非常重要。在我们的病例中,MRI表现的变化有助于诊断垂体脓肿,内镜经蝶窦手术是最佳的手术治疗方法。