scholarly journals Surgical Treatment of Rosai-Dorfman Intracranial Disease: Case Report and Literature Review

2016 ◽  
Vol 37 (03) ◽  
pp. 239-241
Author(s):  
Klisman Hilleshein ◽  
Vinícius Santin ◽  
Fabrício Silva
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Literature Review ◽  
Urinary Retention ◽  
Present Report ◽  
Lymphoproliferative Disease ◽  
Rare Occurrence ◽  
Rosai Dorfman Disease ◽  
Disease Case ◽  
S 100

AbstractRosai-Dorfman disease is a benign lymphoproliferative disease with rare occurrence in the overall population. The characteristic findings of the disease are emperipolesis on microscopy and S-100 protein positivity on immunohistochemistry. The present report describes the case of a 57-year-old man who presented with repeated seizures, urinary retention, and ataxia. Satisfactory results were obtained with surgical treatment. The diagnosis was confirmed by immunohistochemistry.

scholarly journals CAR-T therapy in solid transplant recipients with post-transplant lymphoproliferative disease: case report and literature review

2021 ◽  
Vol 69 (4) ◽  
pp. 103304
Author(s):  
Rafael Hernani ◽  
Asunción Sancho ◽  
Paula Amat ◽  
Juan Carlos Hernández-Boluda ◽  
Ariadna Pérez ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymphoproliferative Disease ◽  
Transplant Recipients ◽  
Post Transplant ◽  
Disease Case ◽  
Car T

Isolated intracranial Rosai-Dorfman disease: Case report and literature review

1998 ◽  
Vol 48 (5) ◽  
pp. 396-402 ◽  
Author(s):  
Hsuan-Ying Huang ◽  
Chao-Cheng Huang ◽  
Cheun-Chung Lui ◽  
Han-Jung Chen ◽  
Wei-Jen Chen
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rosai Dorfman Disease ◽  
Disease Case

scholarly journals HISTOCYTOPATHOLOGICAL DIAGNOSIS OF ROSAI-DORFMAN DISEASE: CASE REPORT AND LITERATURE REVIEW

2021 ◽  
Author(s):  
Zephania Abraham ◽  
Zerd Francis ◽  
Advera Ngaiza ◽  
Aveline Kahinga ◽  
Faustine Bukanu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Sinus Histiocytosis ◽  
Unknown Etiology ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Disease Case

Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self-limiting disease of the cells of macrophage-histiocyte family is of unknown etiology and presents with massive lymphadenopathy. We are hereby reporting a case of RDD presenting with massive bilateral cervical and submandibular lymphadenopathy, diagnosed by histocytopathology.

scholarly journals Tratamiento quirúrgico de la Espondilitis tuberculosa (Enfermedad de Pott). Reporte de un caso y revisión de la literatura. Surgical treatment of tuberculous spondylitis (Pott's disease). Case report and literature review.

2019 ◽  
Vol 30 (2) ◽  
Author(s):  
Nafxiel Jesús Brito-Núñez ◽  
Luis Campos ◽  
Francisco Diaz ◽  
Mariangela Velásquez ◽  
Edenys Izaguire ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Literature Review ◽  
Tuberculous Spondylitis ◽  
Pott’S Disease ◽  
Disease Case

La espondilitis tuberculosa (enfermedad de Pott) representa del 1-5% de los casos de tuberculosis. Se presenta un caso clínico de una paciente femenino de 14 años de edad con espondilitis tuberculosa (enfermedad de Pott) complicada con fractura de cuerpos vertebrales T4, T7, T8 y T9, se realizó un abordaje por vía posterior, consiste en laminectomía completa bilateral de T3, T4, T7, T8, T9 preservando las articulaciones facetarias, mas artrodesis instrumentada con ganchos sublaminares en T1-T2, colocación de alambres sublaminares T5 y T6, tornillos transpediculares en T11 y dos barras de titanio. Con excelentes resultados postoperatorios. Además, se discuten las diferentes vías de abordajes quirúrgicos de esta patología.

Intracranial Rosai–Dorfman disease: Case report and literature review

2010 ◽  
Vol 76 (3) ◽  
pp. e75-e78 ◽  
Author(s):  
Deng XiaoWen ◽  
Xie XueBin ◽  
Ye YuQing ◽  
Liao Ting
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rosai Dorfman Disease ◽  
Disease Case

scholarly journals Solitary Intracranial Rosai-Dorfman Disease: Case Report and Literature Review

2011 ◽  
Vol 39 (5) ◽  
pp. 2045-2050 ◽  
Author(s):  
XY Cao ◽  
SH Luan ◽  
WM Bao ◽  
C Shen ◽  
BJ Yang
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rosai Dorfman Disease ◽  
Disease Case

scholarly journals Rosai-Dorfman Disease Presenting with Solitary Liver Mass Without Lymphadenopathy: Case Report and Literature Review

2021 ◽  
Author(s):  
Yousef Roosta ◽  
Ali Esfahani ◽  
Amir Vahedi ◽  
Kosar Tarvirizadeh ◽  
Sadegh Asoubar ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Plasma Cells ◽  
Protein S ◽  
Liver Mass ◽  
Pathological Study ◽  
Woman Patient ◽  
Rosai Dorfman Disease ◽  
S 100 ◽  
Solitary Liver

This care report presents a 51-year-old woman patient with a cyst-like mass in the liver. The proliferated histiocytes, with the eosinophilic nucleolus, occasionally showing lymphophagocytosis (emperipolesis) positively for CD68 protein S-100 were reported in the pathological study, and the plasma cells were positive for CD138, consistent with Rosai-Dorfman disease.

Spinal Rosai–Dorfman disease: case report and literature review

2017 ◽  
Vol 26 (S1) ◽  
pp. 117-127 ◽  
Author(s):  
Haocheng Xu ◽  
Fan Zhang ◽  
Feizhou Lu ◽  
Jianyuan Jiang
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rosai Dorfman Disease ◽  
Disease Case

scholarly journals Preoperative Diagnosis and Treatment of Middle Ear Adenoma: A Case Report and Literature Review

2021 ◽  
pp. 014556132110002
Author(s):  
Aleksander Zwierz ◽  
Krystyna Masna ◽  
Paweł Burduk
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Literature Review ◽  
Middle Ear ◽  
Surgical Procedures ◽  
Preoperative Diagnosis ◽  
Proper Treatment ◽  
Second Stage ◽  
Middle Ear Adenoma ◽  
Histopathological Results

Most reported cases of middle ear adenoma (MEA) have focused on histopathology because MEA is usually diagnosed postoperatively, which is considered as a major setback. We focused on the surgical aspect of the disease to facilitate a preoperative diagnosis, resulting in prompt and proper treatment, without requiring a second stage of surgical treatment. In this report, we present the differential diagnoses in a 40-year-old man with MEA requiring surgical treatment. Preoperatively, the patient was suspected to have an MEA. An analysis of the surgical procedures in similar misdiagnosed tumors has enabled us to assess surgical procedures in cases wherein the preoperative diagnosis does not coincide with the postoperative histopathological results.

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