Lymphangioleiomyomatosis diagnosed by effusion cytology

A case report

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Lymphangioleiomyomatosis (LAM) is a rare lung disease traditionally affecting women during their childbearing years. It can be sporadic or be associated with tuberous sclerosis syndrome. It is usually manifested in the lungs, kidneys, and/or lymphatic system. It consists of an overgrowth of abnormal smooth muscle-like cells, usually along the bronchovascular structures, resulting in the formation of cysts and the destruction of the lung parenchyma. We present the case of a 43-year-old woman with a history of pleural effusion and dyspnea. A computed tomographic scan revealed a mediastinal mass, chylothorax, and multiple pulmonary cysts. A diagnosis of LAM was rendered on a pleural fluid sample.

Original languageEnglish (US)
Pages (from-to)287-289
Number of pages3
JournalJournal of Cytology
Volume32
Issue number4
DOIs
StatePublished - Oct 1 2015

Fingerprint

Lymphangioleiomyomatosis
Cell Biology
Lung
Cysts
Chylothorax
Lymphatic System
Tuberous Sclerosis
Pleural Effusion
Rare Diseases
Dyspnea
Lung Diseases
Smooth Muscle Myocytes
Kidney

Keywords

  • Lymphangioleiomyomatosis
  • pleural effusion
  • spindle cells
  • tuberous sclerosis

ASJC Scopus subject areas

  • Histology
  • Pathology and Forensic Medicine

Cite this

Lymphangioleiomyomatosis diagnosed by effusion cytology : A case report. / Rivera, Glorimar; Gokaslan, Tunc; Kurian, Elizabeth M.

In: Journal of Cytology, Vol. 32, No. 4, 01.10.2015, p. 287-289.

Research output: Contribution to journalArticle

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