Abstract. Xanthogranuloma, also referred to as cholesterol granuloma or xanthogranulomatous reaction, is a granulomatous lesion that is infrequently found in the sellar and parasellar regions. Xanthogranulomatous pituitary adenoma is relatively rare and, thus, the etiology, diagnosis, management and prognosis of this condition remain incompletely understood. We herein report the case of a 56-year-old female patient who presented to our institution with intermittent headache, vomiting and distending pain in the bilateral orbital regions. Brain magnetic resonance imaging revealed a sellar mass with a heterogeneous signal. The mass was subtotally resected, and histopathological examination confirmed the diagnosis of xanthogranulomatous pituitary adenoma. Although the patient's symptoms were relieved following surgical treatment, intractable hyponatremia and diabetes insipidus developed and she received hormone replacement therapy. At the last follow-up (November 2016), the patient remained recurrence-free. A total of 14 cases of pituitary adenoma with concomitant xanthogranuloma were identified in the literature, and the clinical and radiological manifestations are discussed. Sellar xanthogranuloma is usually associated with craniopharyngioma or Rathke's cleft cyst; however, it may also occur in isolation. Xanthogranulomatous pituitary adenomas are infrequent, making their diagnosis challenging. Surgical resection is the preferred treatment, and attention should be paid to postoperative hypopituitarism and development of diabetes insipidus.
IntroductionSellar xanthogranuloma, also referred to as cholesterol granuloma or xanthogranulomatous reaction, is a rare granulomatous lesion consisting of cholesterol clefts, hemosiderin deposits, macrophages, chronic inflammatory infiltrates and fibrous proliferation (1,2). Sellar xanthogranuloma is most commonly associated with craniopharyngioma or Rathke's cleft cyst, but may also occur in isolation (2). The xanthogranulomatous change was first described in 1988 (3). Xanthogranulomatous pituitary adenomas are extremely rare, with only a few cases reported in the literature to date (1,3,4). Therefore, the etiology, diagnosis, management and prognosis of this condition have yet to be fully elucidated. We herein report a case of pituitary adenoma with concomitant xanthogranuloma in a female patient who developed diabetes insipidus postoperatively. The relevant literature is also reviewed and discussed.
Case reportA 56-year-old woman presented to The First Hospital of Jilin University (Changchun, China) on August 30, 2014, with a 20-day history of intermittent headache, vomiting and distending pain in the bilateral orbital regions. Brain computed tomography (CT) scanning revealed a sellar mass exhibiting heterogeneous hyperintensity (Fig. 1A). Subsequently, brain magnetic resonance imaging (MRI) revealed an intra-and suprasellar oval mass sized 30x25x30 mm, involving the hypothalamus and the foramen of Monro. The pituitary gland and the pituitary stalk could not be clearly ident...