Histiocytosis and storage diseases

Samuel P. Hammar; Timothy C. Allen

doi:10.1007/978-0-387-68792-6_16

Histiocytosis and storage diseases

Samuel P. Hammar, Timothy C. Allen

Research output: Chapter in Book/Report/Conference proceeding › Chapter

6 Scopus citations

Abstract

Histiocytoses of the lung include a variety of diseases for which the unifying characteristic is the accumulation of histiocytic cells within lung parenchyma or air spaces. The diseases include macrophage and dendritic cell disorders as well as storage diseases that result in the accumulation of histiocytic cells in the lung. Pulmonary Langerhans' cell histiocytosis is the most common of these disorders. The histologic, radiologic, immunohistochemical, and, where relevant, ultrastructural characteristics of these diseases are compared in Table 16.1 and discussed in the various sections of this chapter.

Original language	English (US)
Title of host publication	Dail and Hammar's Pulmonary Pathology
Publisher	Springer New York
Pages	600-649
Number of pages	50
Volume	1
ISBN (Print)	9780387983950
DOIs	https://doi.org/10.1007/978-0-387-68792-6_16
State	Published - 2008
Externally published	Yes

ASJC Scopus subject areas

General Medicine

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10.1007/978-0-387-68792-6_16

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abstract = "Histiocytoses of the lung include a variety of diseases for which the unifying characteristic is the accumulation of histiocytic cells within lung parenchyma or air spaces. The diseases include macrophage and dendritic cell disorders as well as storage diseases that result in the accumulation of histiocytic cells in the lung. Pulmonary Langerhans' cell histiocytosis is the most common of these disorders. The histologic, radiologic, immunohistochemical, and, where relevant, ultrastructural characteristics of these diseases are compared in Table 16.1 and discussed in the various sections of this chapter.",

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AB - Histiocytoses of the lung include a variety of diseases for which the unifying characteristic is the accumulation of histiocytic cells within lung parenchyma or air spaces. The diseases include macrophage and dendritic cell disorders as well as storage diseases that result in the accumulation of histiocytic cells in the lung. Pulmonary Langerhans' cell histiocytosis is the most common of these disorders. The histologic, radiologic, immunohistochemical, and, where relevant, ultrastructural characteristics of these diseases are compared in Table 16.1 and discussed in the various sections of this chapter.

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Histiocytosis and storage diseases

Abstract

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