Page 204 - AIDSBK23C
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Page 204


                       IDIOPATHIC THROMBOCYTOPENIC PURPURA.--  There is an increased incidence
               of idiopathic thrombocytopenic purpura (ITP) in patients with HIV infection.  The appearance of
               ITP may precede development of clinical AIDS.  Deposition of circulating immune complexes
               and complement on platelets and/or circulating anti-platelet antibody are thought to be
               mechanisms for HIV-associated ITP.  In cases of refractory ITP, splenectomy has shown to be of
               benefit but with initially higher relapse rates than in persons without HIV infection.[838]

                       HISTOLOGIC PATTERNS.-- A variety of histopathologic patterns of red and white pulp
               may appear in AIDS.  There may be severe lymphocyte depletion with minimal or absent white
               pulp, while in other cases macrophages in small groups or clusters (granulomas) may
               predominate.  In both of these patterns, opportunistic infections or neoplasms are more likely to
               be present.  However, when plasma cells and immunoblasts are prominent in red and/or white
               pulp, infections are not common.  Overall, about 40% of AIDS cases have some opportunistic
               infection or neoplasm involving the spleen.[837]
                       In a majority of persons with AIDS, splenic hemosiderin deposition in red pulp is quite
               prominent.  Iron stains will aid in visualizing these deposits.  Examination of sections by
               polarized light may reveal crystalline birefringent material associated with injection drug use.
               Sometimes large foamy macrophages or multinucleated cells are found without identifiable
               infectious agents.

                       PEDIATRIC FINDINGS.--  At autopsy, young children and infants with HIV infection,
               most of who died from AIDS, may show a variety of histologic changes in the spleen.  These can
               include marked lymphocyte depletion of white pulp and hemophagocytosis.  In addition, about
               half of cases may demonstrate so-called “kaposiform” lesions composed of foci with spindle
               cells admixed with plasma cells, capillaries and hemosiderin-laden macrophages.  Such foci bear
               a resemblance to Kaposi’s sarcoma with marked inflammation.[831]  Splenic smooth muscle
               tumors, including leiomyomas and leiomyosarcomas, can appear in association with childhood
               AIDS and in association with Epstein-Barr virus infection.[589]
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