Angiotropic Lymphoma (Intravascular Lymphomatosis): Description of Two
Cases
Kinkor Z.1, Svitáková I.1, Hadravská Š.2, Hejda V.2, Maťějovič M.3
1Odd. patologie, FN Na Bulovce, Praha 2Šiklův ústav patologie, LF UK, Plzeň 3I. interní klinika, LF UK, Plzeň |
|
Summary:
Described are two cases of angiotropic lymphoma where eventually autopsy elucidated nonspecific
neurologic symptoms. One patient suffering ambiguous encephalitic syndrome died three
months later, the second one passed away after an unusually long three -year period of progressive
dementia and cumulative motoric dysfunction. The autopsy disclosed pure intravascular malignant
lymphoid aggregates (LCA, CD 20, Bcl 2-positive) in the brain and kidney of both patients.
In the patients with the longer disease period, a dissemination to lung was also found. Definitive
diagnosis was issued as a B cell type of angiotropic lymphoma. Skin, lymph nodes, spleen, and
bone marrow were not affected in any case. The clinical differential diagnosis algorithm did not
involve this rare etiology in these particular uncommon neurologic cases and even brain biopsy
performed in both women did not recognize the substantiality of the disease.
Key words:
brain -B cell lymphoma - intravascular lymphomatosis - angiotropic lymphoma - malignant
angioendotheliomatosis
|