| Literature DB >> 15245725 |
Patrick Manckoundia1, Isabelle Rigaud-Royer, Sabine Berthier, Laura Popitean, Bernard Bonnotte, Eve Justrabo, Pierre Pfitzenmeyer, Bernard Lorcerie.
Abstract
Intravascular malignant lymphomatosis (IML) is characterized by proliferation of malignant lymphoid B cells within the lumens of small vessels. Common symptoms include general weakness and central neurological and cutaneous signs. Only histopathological analysis can confirm the diagnosis. We report on a 69-year-old man hospitalized for general weakness, inflammatory syndrome, and hemophagocytic syndrome (HS). Our observation shows that histopathological signs may be observed on a muscular biopsy without clinical or biological signs of muscular involvement.Entities:
Year: 2004 PMID: 15245725 DOI: 10.1016/j.ejim.2004.03.006
Source DB: PubMed Journal: Eur J Intern Med ISSN: 0953-6205 Impact factor: 4.487