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Page 203


               SPLEEN IN AIDS

                       Splenomegaly is a common clinical finding in patients with AIDS, and it is present at
               autopsy in about one third of AIDS cases.  Opportunistic infections or neoplasms are more likely
               to be present when the splenic weight is greater than 400 g.  Weights of up to 1 kg can
               occur.[837]  The most frequent splenic findings at autopsy are M avium complex (MAC), M
               tuberculosis (MTB), cryptococcosis, cytomegalovirus, Kaposi's sarcoma, and malignant
               lymphomas (Table 5).
                       Gross pathologic lesions consist of a prominent follicular pattern in about half of AIDS
               cases and a miliary granulomatous pattern in about 10%.[837]  Sepsis may lead to a soft, almost
               liquid splenic parenchyma.  Splenic infarcts may occur with embolization from non-bacterial
               thrombotic endocarditis or infectious endocarditis involving mitral or aortic valves.

                       OPPORTUNISTIC INFECTIONS.-- Either MAC or MTB can be associated with the
               appearance of granulomas.  Mycobacterium avium complex is more likely to produce a myriad
               of small 0.1 to 0.5 cm soft tan miliary granulomas, while MTB often presents with fewer
               scattered and variably sized granulomas that are tan to white and firm.  Microscopically, MAC
               granulomas are predominantly composed of macrophages filled with numerous mycobacteria.
               Mycobacterium tuberculosis produces a more typical histopathologic appearance with necrosis,
               epithelioid cells, lymphocytes, occasional Langhans' giant cells, and scattered mycobacteria.
                       Cytomegalovirus and Candida are infrequent and difficult to diagnose in spleen.  They
               may be found within small foci of inflammation or necrosis that are not grossly evident and seen
               microscopically only with careful searching at high magnification, aided by methenamine silver
               or PAS stains.
                       The dimorphic fungi C neoformans, H capsulatum, and C immitis may also produce
               visible granulomas but they are never as numerous as the granulomas seen in mycobacterial
               infections.  The fungal organisms are usually distributed throughout the red pulp and are often
               accompanied by proliferations of macrophages.  Diagnosis is facilitated by use of methenamine
               silver or PAS stains.
                       Disseminated P jiroveci (carinii) infection may involve the spleen. By computed
               tomographic scan, multiple nonenhancing, low-density masses with necrosis, hemorrhage, or
               peripheral calcification may be seen.  Grossly, these are large, soft, friable, tan nodules, which
               can have focal hemorrhage.  The same foamy pink exudate seen in pulmonary alveoli is seen
               microscopically, but Gomori methenamine silver staining will demonstrate the cysts, though
               immunoperoxidase staining with monoclonal antibody to P jiroveci (carinii) can be helpful when
               cysts are not readily identified.[416]

                       NEOPLASMS.-- AIDS-associated neoplasms involve the spleen less frequently than
               lymph nodes.  Kaposi's sarcoma can be difficult to diagnose in the spleen because both grossly
               and microscopically, KS can resemble splenic red pulp, and a mass lesion may not be apparent.
               Spindle cells with atypia in a definable nodule or subcapsular infiltrate help to distinguish KS.
               Malignant lymphomas occur in the spleen only one fifth of the time when they are present and
               appear either as nodular masses in regions of white pulp or as infiltrates in red or white pulp.
               The monomorphous nature of lymphomatous infiltrates with large cells is a helpful feature.
               Immunohistochemical staining may be necessary to confirm the diagnosis.
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