Ichtyose acquise révélant une maladie de Hodgkin. Une nouvelle observation

Ennibi, Khalid; Rabhi, M.; Bouzidi, A.; Bahrouch, L.; Boudlal, M.; Ali, Z. Hadj; Akhouad, Y.; Berady, S.; Chaari, J.; Toloune, F.

doi:10.1016/j.revmed.2007.11.015

Cited by 9 publications

(10 citation statements)

References 3 publications

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“…Approximately 80 cases of MPE have been reported in the English literature, and we analyzed the clinical characteristics of 57 cases [3,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33] based on information and articles we found in MEDLINE (table 1). The mean age of MPE patients was 59 years, with similar gender distribution, and the left pleural cavity was more commonly involved.…”

Section: Discussionmentioning

confidence: 99%

Multiple Myeloma with Myelomatous Pleural Effusion: A Case Report and Review of the Literature

Kim¹,

Kim²,

Min³

et al. 2008

Acta Haematol

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Multiple myeloma (MM) is a malignant neoplasm of plasma cell origin. Pleural effusion may develop in the setting of MM due to various reasons, but myelomatous pleural effusion (MPE) is rare. We report a case of MPE in a patient with advanced MM. A 76-year-old woman with MM was admitted to hospital because of dyspnea. Chest X-ray showed right-sided pleural effusion. Protein electrophoresis of the pleural fluid showed monoclonal protein, and cytology demonstrated monoclonal plasma cells. Hospice care was implemented, and the patient died one month later. We present an analysis of the clinical characteristics of 57 MPE cases reported in the English literature. Our review revealed that MPE patients had poor overall survival irrespective of whether MPE develops in the course of their disease or presents as the initial manifestation of MM. Based on this analysis, MPE is a poor prognostic factor, and aggressive treatment should be considered, especially for patients with early-onset MPE.

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Section: Discussionmentioning

confidence: 99%

Multiple Myeloma with Myelomatous Pleural Effusion: A Case Report and Review of the Literature

Kim¹,

Kim²,

Min³

et al. 2008

Acta Haematol

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“…Le diagnostic d'ichtyose est basé sur l'aspect clinique évo-cateur [2]. L'histologie permet de confirmer le diagnostic en montrant l'absence de la couche granuleuse [2]. L'ichtyose acquise révèle fréquemment une maladie sous-jacente [2].…”

Section: Discussionunclassified

“…L'histologie permet de confirmer le diagnostic en montrant l'absence de la couche granuleuse [2]. L'ichtyose acquise révèle fréquemment une maladie sous-jacente [2]. Les hémopathies malignes figurent en première place [2].…”

Section: Discussionunclassified

“…L'ichtyose acquise révèle fréquemment une maladie sous-jacente [2]. Les hémopathies malignes figurent en première place [2]. La maladie de Hodgkin représenterait jusqu'à 80 % des cas [2].…”

Section: Discussionunclassified

“…Les hémopathies malignes figurent en première place [2]. La maladie de Hodgkin représenterait jusqu'à 80 % des cas [2]. Le premier cas d'ichtyose et de maladie de Hodgkin a été décrit en 1925 par Nanta et Chatelier [1,2].…”

Section: Discussionunclassified

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