# Clinical Spectrum of Xeroderma Pigmentosum: An Observational Study

**Authors:** Usha Sri Akkineni, Dilip Chandra Chintada, Kirankanth Vudayana, Pooja Unnikrishnan

PMC · DOI: 10.7759/cureus.93993 · Cureus · 2025-10-07

## TL;DR

This study examines the varied symptoms and cancers in xeroderma pigmentosum patients, emphasizing the need for early diagnosis and sun protection.

## Contribution

The study provides a detailed observational analysis of XP's clinical spectrum, including mucocutaneous and extracutaneous malignancies.

## Key findings

- XP patients showed 100% poikiloderma and 80% freckles, with 20% neurological involvement.
- Common malignancies included squamous cell and basal cell carcinomas, along with extracutaneous cancers like sarcoma and stomach carcinoma.
- Early onset under one year was observed in 70% of cases, highlighting the importance of early diagnosis and cancer screening.

## Abstract

Background

Xeroderma pigmentosum (XP) is an uncommon condition caused by impaired UV radiation-induced damage repair. It is brought on by deficiencies in either post-replication repair or nucleotide excision repair, which can result in neurological, ophthalmic, and cutaneous problems. With a focus on mucocutaneous symptoms, associated malignancies, and systemic involvement, this study aims to record and examine the diverse clinical presentations of XP.

Methodology

A total of 10 clinically diagnosed XP patients participated in this 12-month prospective observational study conducted at a tertiary care center between April 2024 and April 2025. A comprehensive history, consent, and a dermatological, ophthalmic, neurological, and systemic examination were obtained.

Results

Of the 10 cases, there were four (40%) female and 6 (60%) male cases. The age of onset was less than one year in seven (70%) cases, between one and two years in two (20%) cases, and more than two years in one (10%) case. Poikiloderma (10, 100%), freckles (8, 80%), xerosis (8, 80%), lentigenes (6, 60%), skin atrophy (6, 60%), and seborrheic keratosis (4, 40%) were among the cutaneous findings. Neurological involvement was present in two (20%) cases. The ocular findings included photophobia in seven (70%) cases, conjunctival xerosis in six (60%) cases, and cataract in five (50%) cases. Further, two (20%) squamous cell carcinomas, three (30%) basal cell carcinomas, one (10%) lip carcinoma, one (10%) tongue carcinoma, and two (20%) buccal cavity carcinomas were among the mucocutaneous malignancies detected. The extracutaneous cancers observed were one (10%) sarcoma and one (10%) stomach carcinoma.

Conclusions

XP exhibits a wide spectrum of clinical manifestations, including aggressive cancers and pigmentary abnormalities. Enhancing life expectancy and quality of life requires early diagnosis, careful screening for cancer, sun protection, and genetic counseling.

## Linked entities

- **Diseases:** Xeroderma pigmentosum (MONDO:0019600), squamous cell carcinoma (MONDO:0005096), basal cell carcinoma (MONDO:0005341), lip carcinoma (MONDO:0021333), tongue carcinoma (MONDO:0004631), sarcoma (MONDO:0005089), stomach carcinoma (MONDO:0004950)

## Full-text entities

- **Diseases:** Neurological involvement (MESH:C538190), photophobia (MESH:D020795), sarcoma (MESH:D012509), skin atrophy (MESH:D001284), cataract (MESH:D002386), freckles (MESH:D008548), pigmentary abnormalities (MESH:C536859), seborrheic keratosis (MESH:D017492), squamous cell carcinomas (MESH:D002294), tongue carcinoma (MESH:D014062), stomach carcinoma (MESH:D013274), lip carcinoma (MESH:D008048), Poikiloderma (MESH:D011038), basal cell carcinomas (MESH:D002280), XP (MESH:D014983), buccal cavity carcinomas (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12589927/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12589927/full.md

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Source: https://tomesphere.com/paper/PMC12589927