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Intravascular Lymphoma as an Uncommon Cause of Anasarca.
Mylona, Eleni; Golfinopoulou, Styliani; Sfakianaki, Pelagia; Kyriakopoulos, George; Tsonis, Ioannis; Apostolou, Theofanis; Vourlakou, Christina; Skoutelis, Athanasios.
Afiliación
  • Mylona E; Fifth Department of Medicine, Evangelismos General Hospital, Athens, Greece.
  • Golfinopoulou S; Fifth Department of Medicine, Evangelismos General Hospital, Athens, Greece.
  • Sfakianaki P; Fifth Department of Medicine, Evangelismos General Hospital, Athens, Greece.
  • Kyriakopoulos G; Pathology Department, Evangelismos General Hospital, Athens, Greece.
  • Tsonis I; Hematology Department, Evangelismos General Hospital, Athens, Greece.
  • Apostolou T; Nephrology Department, Evangelismos General Hospital, Athens, Greece.
  • Vourlakou C; Pathology Department, Evangelismos General Hospital, Athens, Greece.
  • Skoutelis A; Fifth Department of Medicine, Evangelismos General Hospital, Athens, Greece.
Eur J Case Rep Intern Med ; 3(5): 000424, 2016.
Article en En | MEDLINE | ID: mdl-30755881
ABSTRACT

OBJECTIVES:

To report a case of intravascular lymphoma (IVL) in a Caucasian patient who presented with anasarca as his sole clinical sign. MATERIAL AND

METHODS:

A man presented with anasarca-type oedema and fatigue. After excluding heart failure, hepatic cirrhosis, nephrotic syndrome, hypothyroidism, AL-amyloidosis and adverse drug reaction which can all cause oedema, we turned our attention to capillary permeability disorders.

RESULTS:

Closer review of the bone marrow aspirate demonstrated haemophagocytic histiocytosis, while core, renal and duodenal biopsies showed a B-cell IVL.

CONCLUSION:

The differential diagnosis of anasarca, a relatively common clinical sign, should include IVL although the diagnosis may still be challenging. LEARNING POINTS Anasarca-type oedema is an unusual initial presentation of intravascular lymphoma (IVL) and is normally attributed to capillary permeability disorders.Two clinical forms of IVL have been recognized a Western form and an Asian variant which is characterized by haemophagocytosis.Patients of Caucasian origin who have the clinical features of the Asian variant of IVL make the diagnosis of this condition even more challenging.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Eur J Case Rep Intern Med Año: 2016 Tipo del documento: Article País de afiliación: Grecia

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Eur J Case Rep Intern Med Año: 2016 Tipo del documento: Article País de afiliación: Grecia