ISSN: 1859 - 2872
A case report of eosinophilic multiple membrane effusion accompanying hypereosinophilic syndrome
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Keywords
Hypereosinophilic syndrome, multi-membrane effusion
Abstract
Hypereosinophilic syndrome is a blood disorder characterized by the overproduction of eosinophils in the bone marrow with persistent peripheral eosinophilia, associated with organ damage by the release of eosinophil mediators. As a rare disease, the cause can be caused by allergic, infectious, cancerous and idiopathic diseases. We present a 53-year-old male patient with an absolute eosinophil count of 8910 cells/µL, admitted to the hospital because of abdominal pain, dyspnea, and multi-membrane effusion. Hypereosinophilic syndrome was diagnosed after excluding other causes of eosinophilia. The patient responded completely to corticosteroid therapy.
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References
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4. Crane MM et al (2010) Incidence of myeloproliferative hypereosinophilic syndrome in the United States and an estimate of all hypereosinophilic syndrome incidence. The Journal of allergy and clinical immunology 126(1): 179-181.
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7. Parrillo JE, Fauci AS, Wolff SM (1977) The hypereosinophilic syndrome: dramatic response to therapeutic intervention. Trans Assoc Am Physicians 90: 135-44.
8. Radin M et al (2018) Severe Multi-Organ Failure and Hypereosinophilia: When to Call It "Idiopathic"?. Journal of investigative medicine high impact case reports, 6, 2324709618758347.
9. Simon HU et al (2010) Refining the definition of hypereosinophilic syndrome. J Allergy Clin Immunol 126(1): 45-49.
10. Valent P et al (2012) Contemporary consensus proposal on criteria and classification of eosinophilic disorders and related syndromes. J Allergy Clin Immunol 130(3): 607-612.
11. Zuo L, Rothenberg ME (2007) Gastrointestinal eosinophilia. Immunol Allergy Clin North Am 27(3): 443-555.
12. Ogbogu PU et al (2009) Hypereosinophilic syndromes: A multicenter, retrospective analysis of clinical characteristics and response to therapy. J Allergy Clin Immunol 124(6): 1319-25.e3. doi: 10.1016/j.jaci.2009.09.022.
2. Chusid MJ et al (1975) The hypereosinophilic syndrome: Analysis of fourteen cases with review of the literature. Medicine (Baltimore) 54(1): 1-27.
3. Cogan E, Roufosse F (2012) Clinical management of the hypereosinophilic syndromes. Expert Rev Hematol 5(3): 275-89. quiz 290.
4. Crane MM et al (2010) Incidence of myeloproliferative hypereosinophilic syndrome in the United States and an estimate of all hypereosinophilic syndrome incidence. The Journal of allergy and clinical immunology 126(1): 179-181.
5. Curtis C, Ogbogu P (2016) Hypereosinophilic Syndrome. Clin Rev Allergy Immunol 50(2): 240-251.
6. Moore PM, Harley JB, Fauci AS (1985) Neurologic dysfunction in the idiopathic hypereosinophilic syndrome. Ann Intern Med 102(1): 109-114.
7. Parrillo JE, Fauci AS, Wolff SM (1977) The hypereosinophilic syndrome: dramatic response to therapeutic intervention. Trans Assoc Am Physicians 90: 135-44.
8. Radin M et al (2018) Severe Multi-Organ Failure and Hypereosinophilia: When to Call It "Idiopathic"?. Journal of investigative medicine high impact case reports, 6, 2324709618758347.
9. Simon HU et al (2010) Refining the definition of hypereosinophilic syndrome. J Allergy Clin Immunol 126(1): 45-49.
10. Valent P et al (2012) Contemporary consensus proposal on criteria and classification of eosinophilic disorders and related syndromes. J Allergy Clin Immunol 130(3): 607-612.
11. Zuo L, Rothenberg ME (2007) Gastrointestinal eosinophilia. Immunol Allergy Clin North Am 27(3): 443-555.
12. Ogbogu PU et al (2009) Hypereosinophilic syndromes: A multicenter, retrospective analysis of clinical characteristics and response to therapy. J Allergy Clin Immunol 124(6): 1319-25.e3. doi: 10.1016/j.jaci.2009.09.022.
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Published
Jun 24, 2022
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How to Cite
TháiN. V., TốP. T., ThảoP. T., & HiềuT. V. (2022). A case report of eosinophilic multiple membrane effusion accompanying hypereosinophilic syndrome. Tạp Chí Y Dược lâm sàng 108, 17(4). https://doi.org/10.52389/ydls.v17i4.1241