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Clear Cell Hidradenoma: A Review of Reported Cases
George Ladas1, Christopher Stewart1, Peter A Khoury1
1General Surgery, Kansas City University, Joplin, USA.
Cureus
|February 16, 2026
Summary
Clear cell hidradenoma (CCH) is a rare skin tumor. Larger size and longer growth duration may indicate malignant transformation, particularly in the genitourinary area.
Area of Science:
- Dermatology
- Oncology
- Pathology
Background:
- Clear cell hidradenoma (CCH), also known as acrospiroma, is an infrequent benign skin neoplasm originating from eccrine sweat glands.
- While typically benign, understanding its presentation and malignant potential is crucial for diagnosis and management.
Purpose of the Study:
- To systematically review and analyze the location, occurrence, presentation, and malignant potential of clear cell hidradenoma.
- To identify trends and potential indicators of malignant transformation in CCH.
Main Methods:
- A systematic review of 460 case reports published between 1979 and 2022 using PubMed.
- Adherence to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.
- Extraction of data including demographics, tumor characteristics, location, malignancy status, and progression.
Main Results:
- Analysis included 241 cases of CCH, with an average age of 54.7 years and 54.36% female predominance.
- Thirty-five cases (approximately 14.5%) were malignant, predominantly located in the genitourinary system.
- Malignant CCH showed a statistically significant greater mean length (2 cm) and longer duration of growth (2.75 years) compared to nonmalignant cases.
Conclusions:
- Clear cell hidradenoma is a rare skin tumor, with malignant potential noted, especially in the genitourinary region.
- Tumor size and duration of growth may serve as indicators for malignant transformation.
- Histopathologic examination, biopsy, and surgical excision are recommended for diagnosis and treatment, with awareness of recurrence potential.