A case of hypereosinophilic syndrome presenting with bilateral pleural effusions & recurrent bilateral pneumothoraces

Jae Min Shim; Jin Wook Moon; Sang Yun Hwang; Mi Young Do; Moo Suk Park; Jae Ho Chung; Young Sam Kim; Joon Chang; Sung Kyu Kim; Sang Ho Cho; Se Kyu Kim

doi:10.4046/trd.2004.57.5.470

A case of hypereosinophilic syndrome presenting with bilateral pleural effusions & recurrent bilateral pneumothoraces

Jae Min Shim, Jin Wook Moon, Sang Yun Hwang, Mi Young Do, Moo Suk Park, Jae Ho Chung, Young Sam Kim, Joon Chang, Sung Kyu Kim, Sang Ho Cho, Se Kyu Kim

Research output: Contribution to journal › Review article

Abstract

Idiopathic hypereosinophilic syndrome (HES) is a disorder characterized by prolonged eosinophilia without an identifiable cause and eosinophil related tissue damage in multiple organs including heart, lung, skin, gastrointestinal tract, liver, and the nervous systems. Pulmonary involvement occurs in about 40% of HES cases, but pleural effusion due to pleuritis and bilateral pneumothoraces are very rare manifestations. We report a case of hypereosinophilic syndrome presented with bilateral pleural effusions and recurrent bilateral pneumothoraces in a 44 year-old male with brief review of the literature.

Original language	English
Pages (from-to)	470-475
Number of pages	6
Journal	Tuberculosis and Respiratory Diseases
Volume	57
Issue number	5
DOIs	https://doi.org/10.4046/trd.2004.57.5.470
Publication status	Published - 2004 Nov
Externally published	Yes

Keywords

Hypereosinophilic syndrome
Pleural effusion
Pneumothorax

ASJC Scopus subject areas

Pulmonary and Respiratory Medicine
Infectious Diseases

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Shim, J. M., Moon, J. W., Hwang, S. Y., Do, M. Y., Park, M. S., Chung, J. H., Kim, Y. S., Chang, J., Kim, S. K., Cho, S. H., & Kim, S. K. (2004). A case of hypereosinophilic syndrome presenting with bilateral pleural effusions & recurrent bilateral pneumothoraces. Tuberculosis and Respiratory Diseases, 57(5), 470-475. https://doi.org/10.4046/trd.2004.57.5.470

A case of hypereosinophilic syndrome presenting with bilateral pleural effusions & recurrent bilateral pneumothoraces. / Shim, Jae Min; Moon, Jin Wook; Hwang, Sang Yun; Do, Mi Young; Park, Moo Suk; Chung, Jae Ho; Kim, Young Sam; Chang, Joon; Kim, Sung Kyu; Cho, Sang Ho; Kim, Se Kyu.

In: Tuberculosis and Respiratory Diseases, Vol. 57, No. 5, 11.2004, p. 470-475.

Research output: Contribution to journal › Review article

Shim, Jae Min ; Moon, Jin Wook ; Hwang, Sang Yun ; Do, Mi Young ; Park, Moo Suk ; Chung, Jae Ho ; Kim, Young Sam ; Chang, Joon ; Kim, Sung Kyu ; Cho, Sang Ho ; Kim, Se Kyu. / A case of hypereosinophilic syndrome presenting with bilateral pleural effusions & recurrent bilateral pneumothoraces. In: Tuberculosis and Respiratory Diseases. 2004 ; Vol. 57, No. 5. pp. 470-475.

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abstract = "Idiopathic hypereosinophilic syndrome (HES) is a disorder characterized by prolonged eosinophilia without an identifiable cause and eosinophil related tissue damage in multiple organs including heart, lung, skin, gastrointestinal tract, liver, and the nervous systems. Pulmonary involvement occurs in about 40% of HES cases, but pleural effusion due to pleuritis and bilateral pneumothoraces are very rare manifestations. We report a case of hypereosinophilic syndrome presented with bilateral pleural effusions and recurrent bilateral pneumothoraces in a 44 year-old male with brief review of the literature.",

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AU - Park, Moo Suk

AU - Chung, Jae Ho

AU - Kim, Young Sam

AU - Chang, Joon

AU - Kim, Sung Kyu

AU - Cho, Sang Ho

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AB - Idiopathic hypereosinophilic syndrome (HES) is a disorder characterized by prolonged eosinophilia without an identifiable cause and eosinophil related tissue damage in multiple organs including heart, lung, skin, gastrointestinal tract, liver, and the nervous systems. Pulmonary involvement occurs in about 40% of HES cases, but pleural effusion due to pleuritis and bilateral pneumothoraces are very rare manifestations. We report a case of hypereosinophilic syndrome presented with bilateral pleural effusions and recurrent bilateral pneumothoraces in a 44 year-old male with brief review of the literature.

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