Intravascular lymphomatosis of the T cell type presenting as interstitial lung disease--a case report
Journal of Korean Medical Science
;
: 457-460, 1997.
Article
Dans Anglais
| WPRIM
| ID: wpr-181133
ABSTRACT
Intravascular lymphomatosis (IL) is a rare and generally fatal disease characterized by proliferation of large lymphoma cells almost exclusively within the lumen of small blood vessels. The skin and central nervous systems are typically affected, but involvement of other organs, such as lung, has been described. Predominant lung involvement without cutaneous and neurologic manifestation is very rare and difficult to diagnose. Originally considered as an endothelial disorder, IL has recently been reclassified as lymphoma. Most of the cases reported are of B cell lineage with a few cases of T cell type. We describe a case of the T-cell type IL manifested clinically as an interstitial lung disease without involvement of skin and central nervous systems. Immunohistochemical studies showed the T-cell nature of the neoplastic cells in open lung biopsy sample.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Vaisseaux sanguins
/
Tomodensitomètre
/
Lymphome T
/
Pneumopathies interstitielles
/
Issue fatale
/
Diagnostic différentiel
/
Adulte d'âge moyen
Type d'étude:
Etude diagnostique
Limites du sujet:
Humains
/
Mâle
langue:
Anglais
Texte intégral:
Journal of Korean Medical Science
Année:
1997
Type:
Article
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