Clinical Characteristics and Management of Oral Candidiasis Associated with Calcinosis, Raynaud's Phenomenon, Esophageal Dysmotility, Sclerodactyly, and Telangiectasia Syndrome

Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome, a systemic sclerosis subtype, features skin thickening, vascular issues, and organ involvement, causing complications in the gastrointestinal and musculoskeletal systems. Herein, we present a rare case of oral candidiasis, with CREST syndrome. The patient presented with xerostomia, tongue erythema, and burning pain. The patient reported finger stiffness, facial sclerosis, cold-induced pain, and a 10-year history of palmar-plantar pustulosis. Laboratory tests confirmed antinuclear antibodies (ANA) and anticentromere antibodies (1:1280), leading to a diagnosis of CREST syndrome. A fungal culture identified <i>Candida albicans</i>, and treatment with miconazole gel successfully resolved the infection. This case emphasizes the importance of recognizing oral manifestations in systemic autoimmune diseases, as conditions like xerostomia increase susceptibility to infections.

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Journal
Cureus
Published
2024-12-20
DOI
https://doi.org/10.7759/cureus.76058
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
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article

Clinical Characteristics and Management of Oral Candidiasis Associated with Calcinosis, Raynaud's Phenomenon, Esophageal Dysmotility, Sclerodactyly, and Telangiectasia Syndrome

Fumikazu Sakai, Akiko Okada‐Ogawa, Kana Ozasa, Keita Takizawa et al.
Cureus
Systemic Sclerosis and Related Diseases
article

Clinical Characteristics and Management of Oral Candidiasis Associated with Calcinosis, Raynaud's Phenomenon, Esophageal Dysmotility, Sclerodactyly, and Telangiectasia Syndrome

Fumikazu Sakai, Akiko Okada‐Ogawa, Kana Ozasa, Keita Takizawa, Noboru Noma
article en

Abstract

Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome, a systemic sclerosis subtype, features skin thickening, vascular issues, and organ involvement, causing complications in the gastrointestinal and musculoskeletal systems. Herein, we present a rare case of oral candidiasis, with CREST syndrome. The patient presented with xerostomia, tongue erythema, and burning pain. The patient reported finger stiffness, facial sclerosis, cold-induced pain, and a 10-year history of palmar-plantar pustulosis. Laboratory tests confirmed antinuclear antibodies (ANA) and anticentromere antibodies (1:1280), leading to a diagnosis of CREST syndrome. A fungal culture identified <i>Candida albicans</i>, and treatment with miconazole gel successfully resolved the infection. This case emphasizes the importance of recognizing oral manifestations in systemic autoimmune diseases, as conditions like xerostomia increase susceptibility to infections.

CureusVol. 16(12)
Nihon University (JP)
Zero hunger
Openalex Percentile: Top 62%
Systemic Sclerosis and Related Diseases
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