Immune thrombocytopenic purpura in Hodgkin disease

✍ Scribed by Kamran Hassidim; Robert McMillan; Michael S. Conjalka; John Morrison

• Publisher: John Wiley and Sons
• Year: 1979
• Tongue: English
• Weight: 316 KB
• Volume: 6
• Category: Article
• ISSN: 0361-8609
• DOI: 10.1002/ajh.2830060207

✦ Synopsis

Abstract

Immune thrombocytopenic purpura is rarely seen in Hodgkin disease and the presence of platelet‐associated antibody has not been previously reported in these patients. A patient with Hodgkin disease is described who developed a destructive thrombocytopenia demonstrated by shortened platelet survival. In conjunction with his thrombocytopenia, he had marked elevation of platelet‐associated immunoglobulin G levels (nanograms IgG per 10^9^ platelets: 15,187 prior to splenectomy and 71,130 and 81,900 after surgery). Mean values (± SD) of control subjects averaged 1,975 ± 381 and four patients with Hodgkin disease and normal platelet counts had levels ranging from 1,581 to 4,011.

We suggest that this patient had immune‐mediated thrombocytopenia; whether the increase in platelet‐associated immunoglobulin G was due to antiplatelet antibody or to adsorbed or phagocytosed immune complexes cannot be demonstrated by these studies. The platelet‐associated immunoglobulin G test may be useful in evaluating these patients.