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1. 原発性骨髄線維症における病態 pathogenetic mechanisms in primary myelofibrosis
2. 自己免疫性肝炎の臨床症状および診断 clinical manifestations and diagnosis of autoimmune hepatitis
3. エルドハイム・チェスター病 erdheim chester disease
4. ランゲルハンス細胞組織球症の臨床症状、病理学的特徴、および診断 clinical manifestations pathologic features and diagnosis of langerhans cell histiocytosis

Coexistence of rhinoscleroma with Rosai-Dorfman disease: is rhinoscleroma a cause of this disease?

Kumari JO.SourceDepartment of ENT, Co-Operative Medical College, Kochi, Kerala, India. joku44@yahoo.co.in
The Journal of laryngology and otology.J Laryngol Otol.2012 Jun;126(6):630-2.
INTRODUCTION: Rhinoscleroma and Rosai-Dorfman disease have been reported to coexist in the same patient at different sites. Rosai-Dorfman disease may have an aetiological relationship with rhinoscleroma, although this has not yet been proved.CASE REPORT: A case of a 42-year-old woman with recurrent
PMID 22643208

Emperipolesis: an additional common histopathologic finding in H syndrome and Rosai-Dorfman disease.

Colmenero I, Molho-Pessach V, Torrelo A, Zlotogorski A, Requena L.SourceDepartment of Pathology, Hospital del Niño Jesús, Madrid, Spain.
The American Journal of dermatopathology.Am J Dermatopathol.2012 May;34(3):315-20.
H syndrome is a recently described autosomal recessive disorder characterized by indurated, hyperpigmented, and hypertrichotic cutaneous plaques, mainly involving the lower abdomen and lower extremities. Associated systemic manifestations include hepatosplenomegaly, heart anomalies, hearing loss, hy
PMID 22356918

高木秀雄,西尾仁,後藤哲,森田康太郎,内沢政英,水尾仁志,村上洋平,佐々木豊,森園竜太郎,古山準一
日本消化器病學會雜誌 = The Japanese journal of gastro-enterology 109(7), 1213-1222, 2012-07-05
症例は68歳，女性．C型慢性肝炎を罹患しており，定期検査の際に超音波，造影CT検査で肝細胞癌（S8）および肝門部腫瘤を指摘された．肝動脈化学療法後に肝S8部分切除と肝門部腫瘤摘出術を施行した．肝門部腫瘤は腫大リンパ節であり，病理学的にRosai-Dorfman病類似組織像を呈していた．肝細胞癌との鑑別が困難であった良性リンパ節腫大をともなう症例を経験したので報告する．
NAID 10030803110

Intrathoracic Rosai-Dorfman Disease with Spontaneous Remission : A Clinical Report and a Review of the Literature

NOGUCHI Shingo,YATERA Kazuhiro,SHIMAJIRI Shohei,INOUE Naoyuki,NAGATA Shuya,NISHIDA Chinatsu,KAWANAMI Toshinori,ISHIMOTO Hiroshi,SASAGURI Yasuyuki,MUKAE Hiroshi
Tohoku journal of experimental medicine 227(3), 231-235, 2012-07-01
NAID 10030944015

Intracranial Rosai-Dorfman Disease - a Case Report and a Review of the Literature

Yamauchi Taishi,Hayashi Tomayoshi,Matsuo Takayuki,Matsumoto Miki,Kinoshita Naoe,Abe Kuniko,Nagata Izumi
Acta medica Nagasakiensia 57(2), 57-63, 2012-07-00
… RDD is histologically characterized by emperipolesis,where large histiocytes become infiltrated with lymphocytes and plasma cells. … The tumor consisted of lymphoid tissue with scattered lymph follicles.The infiltrating histiocytes showed emperipolesis. …
NAID 110009442922