A lethal intracranial Rosai‐Dorfman disease of the brainstem diagnosed at autopsy. (16th July 2015)

• Record Type: Journal Article
• Authors: Imada, Hiroki; Sakatani, Takashi; Sawada, Mikio; Matsuura, Tohru; Fukushima, Noriyoshi; Nakano, Imaharu
• Is Part Of: Pathology international. Volume 65:Number 10(2015:Oct.)
• Page Start: 549
• Page End: 553
• Publication Date: 2015-07-16
• Subjects: Pathology -- Periodicals; 616.07
• DOI: 10.1111/pin.12331
• Languages: English
• ISSNs: 1320-5463

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Rosai‐Dorfman disease (RDD) is a benign histiocytic proliferative disorder characterized by the accumulation of histiocytes in lymph nodes and various other organs. RDD seldom involves the central nervous system, and cases of purely intracranial RDD are particularly rare. We report a case of purely intracranial RDD involving the brainstem that was diagnosed at autopsy. A 68‐year‐old woman visited our hospital because of visual disturbances and loss of energy. Magnetic resonance imaging revealed an obscure mass in the brainstem. Despite exhaustive work‐ups, the etiology of the intracranial mass remained unclear. The patient died of respiratory depression, and an autopsy was performed for pathological investigation. Macroscopically, a pink pale mass 2.5 cm in diameter was found in the brainstem, with no attachment to the dura. Histologically, it was composed of histiocytic cells with incorporation of small lymphocytes (emperipolesis). Immunohistochemical staining revealed that the cells were positive for CD68 and S100 and negative for CD1a, consistent with a diagnosis of RDD. Purely intracranial RDD is extremely rare and considered benign. To date, nine cases (including ours) have been reported. To our knowledge, this is the first case of intracranial RDD with autopsy. Although generally considered benign, RDD involving the brainstem might be lethal.</p> </abstract>