HASHIMOTO PRITZKER PDF

E-mail: rb. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This article has been cited by other articles in PMC. Abstract Langerhans cell histiocytosis is a rare, clinically heterogeneous desease. The Hashimoto-Pritzker variant was first described in

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E-mail: rb. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

This article has been cited by other articles in PMC. Abstract Langerhans cell histiocytosis is a rare, clinically heterogeneous desease. The Hashimoto-Pritzker variant was first described in Characteristically, it is present at birth or during the first days of life, impairment is limited to the skin and prognosis is favorable with spontaneous resolution. A variante de Hashimoto-Pritzker foi descrita em First child of healthy and unrelated parents. At birth his mother noticed a 1 x 1. The patient was otherwise healthy.

A second evaluation at age two and a half months showed a complete and spontaneous resolution of the lesion Figure 2. Serologic test for syphilis VDRL was negative both for the mother and the patient. Histopathological exam revealed a dermal infiltrate with predominance of large, round histiocytic cells with dense eosinophilic cytoplasm, with ground glass appearance, and eccentric reniform nuclei Figure 3A. Routine laboratory workup and radiographs of chest, skull, pelvis and long bones were within normal ranges.

The patient remains asymptomatic with no signs of recurrence.

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Langerhans cell histiocytosis

Langerhans Cell Histiocytosis, Hashimoto-Pritzker Type Langerhans Cell Histiocytosis of lung Langerhans Cell Histiocytosis, disseminated clinical Langerhans Cell Histiocytosis, unifocal clinical The disease spectrum results from clonal accumulation and proliferation of cells resembling the epidermal dendritic cells called Langerhans cells , sometimes called dendritic cell histiocytosis. These cells in combination with lymphocytes , eosinophils , and normal histiocytes form typical LCH lesions that can be found in almost any organ. LCH is clinically divided into three groups: unifocal, multifocal unisystem, and multifocal multisystem. It typically has no extraskeletal involvement, but rarely a lesion can be found in the skin, lungs, or stomach.

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Choroba Hashimoto-Pritzkera

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