艾滋病相关的卡波西肉瘤。

AIDS clinical review Pub Date : 1992-01-01
J O Kahn, D W Northfelt, S A Miles
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引用次数: 0

摘要

潜在的免疫抑制程度是AIDS-KS治疗选择的重要考虑因素。一般来说,CD4+ T淋巴细胞大于500/mm3的受试者只需要局部治疗,除非AIDS-KS病变导致某些特定的残疾。CD4+ T淋巴细胞在200 - 500/mm3之间的受试者可能对重组干扰素有应答。该疗法对控制AIDS-KS有效,可与齐多夫定联合使用,并具有抗hiv特性。如果干扰素- α联合齐多夫定在临床上无效,则可能需要全身化疗。AIDS-KS和CD4+ T淋巴细胞低于200/mm3的受试者应接受PCP预防,可能需要全身化疗,并应维持抗逆转录病毒治疗。艾滋病- ks的治疗是不可治愈的,一个潜在的免疫缺陷的治疗计划是必不可少的规划和实施合理的治疗。艾滋病- ks很少危及生命,但通常会在美容和功能上致残。治疗计划仍然侧重于缓解目标,包括减少四肢或面部水肿,消除疼痛病变,缓解艾滋病- ks病变引起的胃肠道紊乱(包括出口梗阻、腹泻和罕见的失血症状),减轻艾滋病- ks的肺负担,以改善氧合和缓解阻塞性肺炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AIDS-associated Kaposi's sarcoma.

The underlying degree of immune suppression is an important consideration in the selection of treatment for AIDS-KS. In general, subjects with CD4+ T lymphocytes greater than 500/mm3 require only local therapy unless there is some specific disability caused by the AIDS-KS lesions. Subjects with CD4+ T lymphocytes between 200 and 500/mm3 may respond to recombinant interferon. This therapy is effective in controlling AIDS-KS, can be combined with zidovudine, and has anti-HIV properties. If interferon-alpha with zidovudine is clinically ineffective, systemic chemotherapy may then be required. Subjects with AIDS-KS and CD4+ T lymphocytes less than 200/mm3 should receive PCP prophylaxis, may require systemic chemotherapy, and should be maintained on antiretroviral therapy. Therapy of AIDS-KS is not curative, and a treatment plan of the underlying immune deficiency is essential for planning and implementing rational therapy. AIDS-KS is rarely life threatening but often cosmetically and functionally disabling. Treatment plans remain focused on palliative goals and include reduction of extremity or facial edema, elimination of painful lesions, relief of gastrointestinal disturbances induced by AIDS-KS lesions (including symptoms of outlet obstruction, diarrhea, and rarely blood loss), and reduction of the pulmonary burden of AIDS-KS to improve oxygenation and relieve obstructive pneumonias.

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