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A lethal intracranial R osai‐ D orfman disease of the brainstem diagnosed at autopsy
Author(s) -
Imada Hiroki,
Sakatani Takashi,
Sawada Mikio,
Matsuura Tohru,
Fukushima Noriyoshi,
Nakano Imaharu
Publication year - 2015
Publication title -
pathology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
eISSN - 1440-1827
pISSN - 1320-5463
DOI - 10.1111/pin.12331
Subject(s) - emperipolesis , autopsy , pathology , medicine , brainstem , cd68 , rosai–dorfman disease , immunohistochemistry , pathological , histiocyte , etiology
R osai‐ D orfman 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 CD 68 and S 100 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.