Abstract
Histiocytic syndromes represent a large, heterogeneous group of diseases resulting from proliferation of histiocytes. In addition to the classic variants, the subset of non-Langerhans cell histiocytoses comprises rare entities that have more recently been described. These last include both forms that affect only the skin or the skin and mucous membranes, and usually show a benign clinical behavior, and forms involving also internal organs, which may follow an aggressive course. The goal of this review is to outline the clinical, histologic, and ultrastructural features and the course, prognosis, and management of these unusual histiocytic syndromes.
| Original language | English |
|---|---|
| Pages (from-to) | 1031-1045 |
| Number of pages | 15 |
| Journal | Journal of the American Academy of Dermatology |
| Volume | 57 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - Dec 2007 |
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ASJC Scopus subject areas
- Dermatology
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Unusual variants of non-Langerhans cell histiocytoses. / Caputo, Ruggero; Marzano, Angelo Valerio; Passoni, Emanuela; Berti, Emilio.
In: Journal of the American Academy of Dermatology, Vol. 57, No. 6, 12.2007, p. 1031-1045.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Unusual variants of non-Langerhans cell histiocytoses
AU - Caputo, Ruggero
AU - Marzano, Angelo Valerio
AU - Passoni, Emanuela
AU - Berti, Emilio
PY - 2007/12
Y1 - 2007/12
N2 - Histiocytic syndromes represent a large, heterogeneous group of diseases resulting from proliferation of histiocytes. In addition to the classic variants, the subset of non-Langerhans cell histiocytoses comprises rare entities that have more recently been described. These last include both forms that affect only the skin or the skin and mucous membranes, and usually show a benign clinical behavior, and forms involving also internal organs, which may follow an aggressive course. The goal of this review is to outline the clinical, histologic, and ultrastructural features and the course, prognosis, and management of these unusual histiocytic syndromes.
AB - Histiocytic syndromes represent a large, heterogeneous group of diseases resulting from proliferation of histiocytes. In addition to the classic variants, the subset of non-Langerhans cell histiocytoses comprises rare entities that have more recently been described. These last include both forms that affect only the skin or the skin and mucous membranes, and usually show a benign clinical behavior, and forms involving also internal organs, which may follow an aggressive course. The goal of this review is to outline the clinical, histologic, and ultrastructural features and the course, prognosis, and management of these unusual histiocytic syndromes.
UR - http://www.scopus.com/inward/record.url?scp=36148991854&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=36148991854&partnerID=8YFLogxK
U2 - 10.1016/j.jaad.2007.03.014
DO - 10.1016/j.jaad.2007.03.014
M3 - Article
C2 - 17485142
AN - SCOPUS:36148991854
VL - 57
SP - 1031
EP - 1045
JO - Journal of the American Academy of Dermatology
JF - Journal of the American Academy of Dermatology
SN - 0190-9622
IS - 6
ER -