# A Rare Constellation of Triple Cutaneous Malignancies With Sustained Therapeutic Response: Kaposi Sarcoma, Basal Cell Carcinoma, and Cutaneous Squamous Cell Carcinoma in a Single Patient

**Authors:** Ivan Bivolarski

PMC · DOI: 10.7759/cureus.94604 · 2025-10-14

## TL;DR

An 83-year-old man developed three rare skin cancers simultaneously and showed a long-term response to treatment, highlighting the challenges and possible shared causes of these conditions.

## Contribution

This case report documents the rare co-occurrence of Kaposi sarcoma, BCC, and cSCC in one patient and their sustained response to multimodal therapy.

## Key findings

- The patient had three distinct skin malignancies confirmed histopathologically.
- He achieved sustained therapeutic benefit for over 18 months with multimodal treatment.
- The case suggests overlapping carcinogenic mechanisms like viral infection and immune dysregulation.

## Abstract

The simultaneous occurrence of three distinct cutaneous malignancies - Kaposi sarcoma (KS), basal cell carcinoma (BCC), and cutaneous squamous cell carcinoma (cSCC) - in a single patient is exceptionally uncommon. We report the case of an 83-year-old male with cardiovascular comorbidities who was diagnosed with KS following histopathological confirmation (CD34⁺, ERG⁺, HHV-8⁺) and had a prior history of excised BCC and cSCC of the skin between 2020 and 2022. Over the course of his illness, he underwent multiple surgical resections, axillary lymph node dissection, systemic chemotherapy with paclitaxel, and immunotherapy. Despite eventual disease progression, he achieved sustained therapeutic benefit for more than 18 months, with clinical stabilization of lesions and meaningful palliation.

This rare constellation underscores the diagnostic and therapeutic challenges of managing multiple primary skin malignancies in an immunosenescent patient. The coexistence of KS with keratinocyte carcinomas may reflect overlapping carcinogenic mechanisms, including viral oncogenesis (human herpesvirus-8 (HHV-8)), ultraviolet exposure, and immune dysregulation. Vigilant lesion-by-lesion biopsy, histopathological confirmation, and individualized multimodal management can achieve durable disease control and improved quality of life, even in elderly patients with complex dermatologic oncologic presentations.

## Linked entities

- **Proteins:** CD34 (CD34 molecule), ERG (ETS transcription factor ERG)
- **Chemicals:** paclitaxel (PubChem CID 36314)
- **Diseases:** Kaposi sarcoma (MONDO:0005055), basal cell carcinoma (MONDO:0005341), cutaneous squamous cell carcinoma (MONDO:0002529)

## Full-text entities

- **Genes:** ERG (ETS transcription factor ERG) [NCBI Gene 2078] {aka LMPHM14, erg-3, p55}, CD34 (CD34 molecule) [NCBI Gene 947]
- **Diseases:** immune dysregulation (OMIM:614878), KS (MESH:D012514), Cutaneous Squamous Cell Carcinoma (MESH:D002294), BCC (MESH:D002280), keratinocyte carcinomas (MESH:C580062), dermatologic oncologic (MESH:D000072716), Cutaneous Malignancies (MESH:C562393), skin malignancies (MESH:D009369)
- **Chemicals:** paclitaxel (MESH:D017239)
- **Species:** Human gammaherpesvirus 8 (no rank) [taxon 37296], Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12615987/full.md

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Source: https://tomesphere.com/paper/PMC12615987