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Malignant Hidradenocarcinoma Initially Diagnosed as an Apocrine Hidrocystoma: a Case Report and Literature Review

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Abstract

Hidradenocarcinoma is a rare malignant tumor with an aggressive clinical course, and it accounts for < 0.05% of all malignant tumors. It is known to mainly develop de novo, and rarely seen observed to arise from an existing hidradenoma. In this report, we describe a rare case of hidradenocarcinoma that was initially diagnosed as an apocrine hidrocystoma on punch biopsy. During follow-up, the lesion recurred, and complete excision biopsy confirmed the diagnosis of hidradenocarcinoma. Because of the aggressive nature of the disease, we performed wide excision of the lesion, and the defect was reconstructed with a thin free anterolateral thigh perforator flap. No evidence of recurrence was observed during the 11-month follow-up period.

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Authors

Contributions

Conceptualization, defining of study: JHL

Operative work: JSC, NRK, JHL

Data acquisition and analysis: JSC, JAK

Manuscript writing: JSC, NRK, JAK, JHL

Corresponding author

Correspondence to Jung Ho Lee.

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The authors declare that they have no conflict of interest.

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Informed consent was obtained from the participant included in the study.

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Choi, J.S., Kim, N.R., Kim, J.A. et al. Malignant Hidradenocarcinoma Initially Diagnosed as an Apocrine Hidrocystoma: a Case Report and Literature Review. Indian J Surg 82, 969–972 (2020). https://doi.org/10.1007/s12262-020-02193-z

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  • DOI: https://doi.org/10.1007/s12262-020-02193-z

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