Pulmonary Langerhans Cell Histiocytosis Masquerading as Lymphangioleiomyomatosis

被引：0

作者：

Patel, Priya ^{[1
]}

Anamika, F. N. U. ^{[2
]}

Ali, Rana ^{[3
]}

机构：

[1] Hackensack Meridian Hlth Ocean Univ Med Ctr, Sleep Med, Brick Township, NJ 08724 USA

[2] Hackensack Meridian Hlth Ocean Univ Med Ctr, Internal Med, Brick Township, NJ USA

[3] Hackensack Meridian Hlth Ocean Univ Med Ctr, Pulm & Sleep Med, Brick Township, NJ USA

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2023年 / 15卷 / 05期

关键词：

lam; plch; diffuse lung disease; cigarette smoking; lung cysts; EOSINOPHILIC GRANULOMA; LUNG;

D O I：

10.7759/cureus.38486

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Pulmonary Langerhans cell histiocytosis (PLCH) is an uncommon lung disease that affects young adults aged 20 to 40 years with current or prior history of smoking. The pathologic cell type in PLCH is a dendritic cell of the monocyte-macrophage line that resembles cutaneous Langerhans cells. This report presents the case of a 42-year-old woman with PLCH. We discuss her clinical symptoms, diagnostic tests, and treatment plan, with a specific focus on the radiologic features. The patient exhibited a radiologic appearance similar to that of lymphangiomyomatosis with histologic evidence of PLCH.

引用

页数：4

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