- Emperipolesis within Megakaryocyte in Hepatic Hemopoiesis
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Kim DJ, Yang HC, Ahn JK, Kim SS, Kim KY, Lee WB
- KMID: 2092693
- Korean J Anat.
- 1999 Oct;32(5):593-604.
This study is designed to detect the emperipolesis in megakaryocyte in fetal liver, which is an important organ of hemopoiesis, during rat development, and to compare the activity of erythropoiesis... -
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- Erdheim-Chester Disease with Emperipolesis: A Unique Case Involving the Heart
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Zhu P, Li N, Yu L, Miranda MN, Wang G, Duan Y
- KMID: 2378129
- Cancer Res Treat.
- 2017 Apr;49(2):553-558.
- doi: 10.4143/crt.2016.078
Histiocytosis is an uncommon disease characterized by excessive accumulation of histiocytes. Here, we report a rare case of non-Langerhans-cell histiocytosis in a 51-year-old woman who presented with severe symptoms of... -
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- Immunohistochemical and Transmission Electron Microscopic Studies of Erythroblastic Islands in Human Fetal Liver
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Kim HY, Chae HS, Kim YW, Kim KY, Lee WB
- KMID: 1530057
- Korean J Anat.
- 1998 Apr;31(2):205-216.
Macrophages in 14 human livers from 5 to 37 weeks of gestation were studied immunohistochemically and transmission electron microscopically with 3 human fetal livers during the high activity of hepatic... -
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- Isolated Intracranial Rosai-Dorfman Disease: A Case Report
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Park JK, Cho MY, Park KH, Pyen JS
- KMID: 2277701
- Korean J Pathol.
- 2004 Dec;38(6):430-433.
Rosai-Dorfman disease (RDD) is an idiopathic histioproliferative disorder of the lymph nodes and extranodal sites. Central nervous system involvement is extremely rare. Intracranial RDD, especially the isolated form, resembles meninigioma... -
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- Cutaneous Rosai-Dorfman Disease Confused with Vascular Mass
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Kang KR, Jung SW, Koh SH
- KMID: 2159966
- Arch Craniofac Surg.
- 2016 Mar;17(1):31-34.
- doi: 10.7181/acfs.2016.17.1.31
Rosai-Dorfman disease is a rare histiocytic disorder, clinically characterized by massive, bilateral painless cervical lymphadenopathy with potential for extranodal manifestations. We report a 45-year-old male patient who presented with a... -
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- Development and Migration of Megakaryocyte during Hepatic Hemopoiesis in Human Fetuses
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Lee WB, Lee CW, Chung BS, Kim BS, Kim DJ, Kim SS, Kim KY
- KMID: 1559311
- Korean J Anat.
- 2002 Aug;35(4):285-296.
Liver tissuses obtained from 5 human fetuses between 11 weeks and 23 weeks of gestation during the high activity of hepatic hemopoiesis were observed with transmission electron microscope using continuous... -
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- Rosai-Dorfman disease of soft tissue
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Song SE, Lim TW, Lee KJ, Jo AR, Chae BD, Ko MJ, Lee CW
- KMID: 2319911
- Yeungnam Univ J Med.
- 2015 Dec;32(2):114-117.
- doi: 10.12701/yujm.2015.32.2.114
Rosai-Dorfman disease (RDD) is a benign proliferative histiocytic disorder of unknown etiology, which typically manifests as lymphadenopathy and systemic symptoms. Lymph node involvement is typical, but soft tissue RDD without... -
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- Migration of Emperipoletic Erythroblasts Within Kupffer Cells in Human Hepatic Hemopoiesis: Electron Microscopic Study
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Lee WB, Yoo DH, Chae HS, Bach JH, Kim SS, Kim KY
- KMID: 1559109
- Korean J Anat.
- 2001 Jun;34(3):231-244.
The presence of erythroblasts within Kupffer cell was studied for transmission electron microscopically with 5 human fetal livers from 11 to 23 weeks of gestation during the high activity of... -
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- 1 Case: Pulmonary Giant Cell Carcinoma
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Kim HG, Choi YH, Hwang JJ, Kim OJ, Kim HJ
- KMID: 1915504
- Korean J Thorac Cardiovasc Surg.
- 1999 Feb;32(2):185-188.
The pulmonary giant cell carcinoma is classified as a variant of a large cell carcinoma and is diagnosed by the minimum component of 10% huge, pleomorphic and multinucleated giant tumor... -
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- Rosai-Dorfman Disease in Thoracic Spine: A Rare Case of Compression Fracture
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Kim DY, Park JH, Shin DA, Yi S, Ha Y, Yoon DH, Kim KN
- KMID: 1885679
- Korean J Spine.
- 2014 Sep;11(3):198-201.
- doi: 10.14245/kjs.2014.11.3.198
Sinus histiocytosis with massive lymphadenopathy known as Rosai-Dorfman disease is characterized by painless bilateral cervical lymphadenopathy. Extranodal manifestations are uncommon and spinal involvement is rare. A 15-year-old man presented with... -
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- Rosai-Dorfman Disease in the Breast with Increased IgG4 Expressing Plasma Cells: A Case Report
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Cha YJ, Yang WI, Park SH, Koo JS
- KMID: 2277491
- Korean J Pathol.
- 2012 Oct;46(5):489-493.
Rosai-Dorfman disease (RDD) can present in any anatomic site, but breast involvement is rarely reported. Recently, a relationship between RDD and IgG4-related sclerosing disease has been suggested. Here we report... -
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- A Case of Rosai-Dorfman Disease Treated with Hydroxychloroquine
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Baek JO, Lee HY, Lee JR, Kim M, Roh JY, Kim YC
- KMID: 2302140
- Korean J Dermatol.
- 2007 Oct;45(10):1055-1059.
Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy (SMHL) is a benign histiocytic proliferative disorder of unknown etiology. It is accompanied by fever, leukocytosis, elevated erythrocyte sedimentation rate and polyclonal... -
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- A Case of Cutaneous Rosai-Dofman Disease Treated with Isotretinoin and Pulsed Dye Laser
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Han J, Kim JE, Park GH, Won CH, Chang SE, Lee MW, Choi JH, Moon KC
- KMID: 2388401
- Korean J Dermatol.
- 2013 Jun;51(6):465-469.
Rosai-Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy (SMHL) is a benign histiocytic proliferative disorder of unknown etiology. The disease is usually accompanied by massive bilateral lymphadenopathy, fever, elevated... -
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- Rosai-Dorfman Disease with Massive Cutaneous Nodule on the Shoulder and Back
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Ma H, Zheng Y, Zhu G, Wu J, Lu C, Lai W
- KMID: 2264840
- Ann Dermatol.
- 2015 Feb;27(1):71-75.
- doi: 10.5021/ad.2015.27.1.71
Rosai-Dorfman disease is a rare, idiopathic, benign, and self-limiting histiocytic proliferative disorder. A 26-year-old man presented with a single massive cutaneous nodule (reaching 30 cm in diameter) on the left... -
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