# Are Corticosteroids Truly Contraindicated in Pulmonary Kaposi Sarcoma?

**Authors:** Sai Anoosh Parimi, Bryan K Dunn

PMC · DOI: 10.7759/cureus.102101 · 2026-01-22

## TL;DR

This paper discusses a case where corticosteroids improved respiratory failure in a patient with pulmonary Kaposi sarcoma, challenging traditional beliefs about their use.

## Contribution

The paper presents a novel case report suggesting corticosteroids may be beneficial in pulmonary Kaposi sarcoma when used judiciously.

## Key findings

- The patient showed significant improvement in respiratory failure after treatment with corticosteroids and paclitaxel.
- This case challenges the traditional view that corticosteroids exacerbate Kaposi sarcoma in HIV/AIDS patients.

## Abstract

Kaposi sarcoma (KS) is an angioproliferative disorder associated with human herpes virus 8 (HHV-8) infection. It has both cutaneous and extracutaneous manifestations. With extracutaneous manifestations, it most commonly involves the oral cavity, gastrointestinal tract, and regional lymph nodes. Visceral organ involvement other than the gastrointestinal tract, such as the liver, lungs, and bones, is extremely rare. Here, we would like to discuss a patient with human immunodeficiency virus (HIV) and acquired immunodeficiency syndrome (AIDS) found to have pulmonary KS manifesting as acute hypoxemic respiratory failure (AHRF), along with bilateral pleural effusions and endobronchial lesions confirmed on bronchoscopy. He was treated with corticosteroids and paclitaxel, with significant improvement in AHRF. Traditionally, corticosteroids have been associated with exacerbation of pre-existing KS and even development of new-onset KS in HIV-infected patients and induction of KS. The experience gained from this case report suggests that judicious use of corticosteroids may improve the outcome of pulmonary dysfunction in HIV/AIDS-associated KS patients.

## Linked entities

- **Chemicals:** paclitaxel (PubChem CID 36314)
- **Diseases:** Kaposi sarcoma (MONDO:0005055)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}
- **Diseases:** cough (MESH:D003371), atelectasis (MESH:D001261), blood-tinged sputum (MESH:D006402), death (MESH:D003643), erythema (MESH:D004890), HIV (MESH:D015658), fungal (MESH:D009181), infectious disease (MESH:D003141), wheezing (MESH:D012135), pulmonary (MESH:D008171), cancer (MESH:D009369), opportunistic infections (MESH:D009894), Adenopathy (MESH:D000072281), dyspnea (MESH:D004417), IRIS (MESH:D054019), PJP (MESH:D011020), mucocutaneous (MESH:D007897), inflammatory (MESH:D007249), fevers (MESH:D005334), respiratory distress (MESH:D012128), Endobronchial obstruction (MESH:D000402), pulmonary dysfunction (MESH:D011660), hypoxemia (MESH:D000860), KS (MESH:D012514), angioproliferative disorder (MESH:D009358), oral lesions (MESH:D009059), febrile (MESH:D000071072), lymphadenopathy (MESH:D008206), AHRF (MESH:D012131), AIDS (MESH:D000163), Pleural effusions (MESH:D010996), pneumonia (MESH:D011014), hemoptysis (MESH:D006469), cachexia (MESH:D002100), fatigue (MESH:D005221), wasting (MESH:D019282)
- **Chemicals:** FiO2 (-), doxorubicin (MESH:D004317), paclitaxel (MESH:D017239), bictegravir (MESH:C000620396), azithromycin (MESH:D017963), oxygen (MESH:D010100), tenofovir alafenamide (MESH:C442442), piperacillin (MESH:D010878), bictegravir/emtricitabine/tenofovir alafenamide (MESH:C000654125), tazobactam (MESH:D000078142), methylprednisolone (MESH:D008775), cefepime (MESH:D000077723), vancomycin (MESH:D014640)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus (species) [taxon 12721], Human gammaherpesvirus 8 (no rank) [taxon 37296], Pneumocystis (genus) [taxon 4753], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12924720/full.md

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Source: https://tomesphere.com/paper/PMC12924720