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Generalized Cytomegalic Inclusion DiseaseGeneral and Dermatologic Aspects with Report of a Case
ROGER H. BRODKIN, M.D.;
MORTON WEINBERG, M.D.;
MORRIS LEIDER, M.D.
Arch Dermatol. 1961;84(4):650-653.
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In the past 10 years articles have been appearing regularly in the pediatric literature that describe a likely entity, now titled generalized cytomegalic inclusion disease, which seems to be a viral infection principally of infants.1-5 As in other systemic diseases, the skin may partake in the process and then may bear signs on or in it that are readily apparent either to the examining eye grossly or upon microscopy. Those signs are icterus and forms of contained hemorrhage (petechiae and purpura). The dermatologist who is knowledgeable of the condition may thus at times, in an appropriate case showing jaundice and petechiae or purpura, be able to suggest the possibility of generalized cytomegalic inclusion disease among other differential possibilities, and, if correct, the diagnosis may then be conclusively established by more or less simple laboratory procedures, especially search for characteristic inclusion bodies within epithelial cells found in urine sediment.
Report
. . . [Full Text PDF of this Article]
Author Affiliations
NEW YORK
From the Department of Dermatology of the New York University Post-Graduate Medical School and the Service of Dermatology of Bellevue Hospital.
Footnotes
Submitted for publication June 2, 1961.
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