The Experts below are selected from a list of 360 Experts worldwide ranked by ideXlab platform
Xiangsong Zhang - One of the best experts on this subject based on the ideXlab platform.
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18f fdg pet ct findings in multicentric Reticulohistiocytosis
Clinical Nuclear Medicine, 2016Co-Authors: Bing Zhang, Hui Zhou, Jiande Han, Xinchong Shi, Xiangsong ZhangAbstract:Multicentric Reticulohistiocytosis is a rare systemic inflammatory disease of unknown etiology characterized by the infiltration of histiocytes and multinucleated giant cells into multiple systems. The definitive diagnosis depends on biopsy of the affected tissues. Here, we report the F-FDG PET/CT findings of a 62-year-old man with multicentric Reticulohistiocytosis. Increased FDG uptake was observed in cutaneomucosal papules, surrounding tissues of many joints, multiple muscles, and lymph nodes.
Young C Kauh - One of the best experts on this subject based on the ideXlab platform.
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solitary congenital self healing Reticulohistiocytosis
British Journal of Dermatology, 1993Co-Authors: E F Bernstein, K S Resnik, J H Loose, C Halcin, Young C KauhAbstract:Congenital self-healing Reticulohistiocytosis (CSHR) was first described in 1973 by Hashimoto and Pritzker. Since then, both multiple and solitary forms have been described. We report a further case of solitary congenital self-healing Reticulohistiocytosis. CSHR is a rare disorder which frequently presents a diagnostic dilemma in the newborn. Nodular forms of systemic Langerhans cell histiocytosis may present in a manner similar to CSHR. Because their differentiation on histopathological grounds is impossible, physical examination, laboratory investigations, and follow-up are necessary to ensure a lack of systemic involvement. Although previously thought to represent a rare variant of CSHR, solitary lesions of CSHR account for almost 25% of reported cases. A review of the literature relating to solitary CSHR, and a consideration of the differential diagnosis of a solitary congenital nodule, are also presented.
Bing Zhang - One of the best experts on this subject based on the ideXlab platform.
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18f fdg pet ct findings in multicentric Reticulohistiocytosis
Clinical Nuclear Medicine, 2016Co-Authors: Bing Zhang, Hui Zhou, Jiande Han, Xinchong Shi, Xiangsong ZhangAbstract:Multicentric Reticulohistiocytosis is a rare systemic inflammatory disease of unknown etiology characterized by the infiltration of histiocytes and multinucleated giant cells into multiple systems. The definitive diagnosis depends on biopsy of the affected tissues. Here, we report the F-FDG PET/CT findings of a 62-year-old man with multicentric Reticulohistiocytosis. Increased FDG uptake was observed in cutaneomucosal papules, surrounding tissues of many joints, multiple muscles, and lymph nodes.
Jean Sibilia - One of the best experts on this subject based on the ideXlab platform.
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multicentric Reticulohistiocytosis an autoimmune systemic disease case report of an association with erosive rheumatoid arthritis and systemic sjogren syndrome
Joint Bone Spine, 2010Co-Authors: Kaouther Ben Abdelghani, I Mahmoud, Emmanuel Chatelus, Christelle Sordet, Jacqueseric Gottenberg, Jean SibiliaAbstract:Multicentric Reticulohistiocytosis is a rare, systemic, reactive histiocytic disease of unknown aetiology. Autoimmune diseases have previously been reported in association with multicentric Reticulohistiocytosis, but whether this is a true association or mere coincidence is not known. Here, we report the case of a 50-year-old woman who had been diagnosed as suffering from rheumatoid arthritis (RA), four years ago with positive rheumatoid serology was evaluated for multiple asymptotic papulonodules eruption. Histopathologic examination was suggestive of multicentric Reticulohistiocytosis. She developed concomitantly Sjogren syndrome with systemic manifestations. Multicentric Reticulohistiocytosis may be misdiagnosed as RA, but evaluation of the time course of specific symptoms can greatly help in the correct diagnosis. The possibility of commune etiopathogeny of these affections is discussed.
Andrea L. Zaenglein - One of the best experts on this subject based on the ideXlab platform.
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Congenital self-healing Reticulohistiocytosis.
The Journal of clinical and aesthetic dermatology, 2014Co-Authors: Young H. Lee, Mala K. Talekar, Catherine G. Chung, Moshe D. Bell, Andrea L. ZaengleinAbstract:Congenital self-healing Reticulohistiocytosis, also known as congenital self-healing Langerhans cell histiocytosis or Hashimoto-Pritzker disease, is a Langerhans cell histiocytosis. It is characterized by skin lesions in the newborn period in an otherwise healthy infant that show a Langerhans cell infiltrate in the skin on histological analysis. These findings subsequently spontaneously involute. This report describes two newborns who presented at birth with differing presentations of congenital self-healing Reticulohistiocytosis. A review of the disorder, including diagnosis and evaluation, is presented.