The association of hyperglobulinemia with large lymphangiomas or with extensive lymphangiectasia, as in Milroy's disease, has been recorded, but to our knowledge, no studies on the nature of this association have been published. "Sequestration" of blood platelets by hemangiomas with resultant thrombocytopenic purpura, anemia due to chronic blood loss from ulcerated superficial hemangiomas, and protein depletion due to gastrointestinal lymphatic obstruction by mesenteric lymphangioma represent additional examples of system effects of angiomas. The present paper describes studies on an infant with hyperglobulinemia and a large cavernous lymphangioma and discusses the possible causes of the phenomenon.
Report of a Case
A white female infant, born Feb. 26, 1957, was first admitted to the Cincinnati Children's Hospital on Aug. 31, 1958. At birth, she was found to have massive lymphangiomatosis of the right foot, leg, and buttock (Fig. 1). During infancy there were episodes of infection of the affected leg, but
JONES DV, LONGACRE JJ, LANDING BH, WITTGENSTEIN E. Hyperglobulinemia Secondary to Massive Lymphangioma. Am J Dis Child. 1961;101(4):510–513. doi:10.1001/archpedi.1961.04020050100015