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Images in Clinical Practice
89 (
4
); 613-614
doi:
10.25259/IJDVL_1026_2021
pmid:
35389033

Giant proliferating trichilemmal tumour of the scalp

Department of Plastic and Reconstructive Surgery, Kangwon National University, School of Medicine, Kanwondaehak-gil 1, Chuncheon, Kangwon-do, Republic of Korea
Department of Anatomic Pathology, Kangwon National University, School of Medicine, Kanwondaehak-gil 1, Chuncheon, Kangwon-do, Republic of Korea
Department of Plastic and Reconstructive Surgery, Kangwon National University Hospital, Baekryeong-ro 156, Chuncheon, Kangwon-do, Republic of Korea

Corresponding author: Dr. Sang-Yeul Lee, Department of Plastic and Reconstructive Surgery, Kangwon National University Hospital, Baekryeong-ro 156, Chuncheon, Kangwon-do, Republic of Korea. serafin5@unitel.co.kr

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

An 88-year-old woman presented with a large, asymptomatic, slow-growing scalp mass that had been persisting for over 40 years. Physical examination revealed a flesh-coloured, dome-shaped mass with ulceration and haemorrhagic crusting in the occipital region, measuring 8 × 5 × 3.5 cm [Figure 1]. The tumour was resected with a 10 mm margin of normal scalp tissue over the pericranium. Histopathologically, the lesion showed squamous epithelial proliferation and trichilemmal keratinization, with no evidence of malignancy or local invasion. Proliferating trichilemmal tumours are uncommon adnexal neoplasms frequently occurring on the scalp, usually benign but with locally invasive and even metastatic potential. Abnormally large proliferating trichilemmal tumours, described as giant proliferating trichilemmal tumours, commonly have long clinical histories and develop skin changes such as ulceration and necrosis. The clinical features that predict a risky prognosis include a rapid increase in size, tumour size greater than 5 cm, non-scalp location and foci of necrosis or ulceration. Complete surgical excision of the tumour with a 1 cm margin of normal tissue is the proper therapy to prevent local recurrence.

A flesh-coloured, dome-shaped mass (8 × 5 × 3.5 cm) with ulceration and haemorrhagic crusting in the occipital region
Figure 1
A flesh-coloured, dome-shaped mass (8 × 5 × 3.5 cm) with ulceration and haemorrhagic crusting in the occipital region

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.


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