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SKINDIA QUIZ |
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Year : 2020 | Volume
: 11
| Issue : 4 | Page : 665-666 |
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Chronic anogenital ulceration
Ömer Kutlu, Fatma Nur Kutlu, Yücel Tekin
Uşak University, School of Medicine, Department of Dermatology and Venereology, Uşak, Turkey
Date of Web Publication | 13-Jul-2020 |
Correspondence Address: Ömer Kutlu Usak University, School of Medicine, Department of Dermatology and Venereology, Usak Turkey
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/idoj.IDOJ_121_19
How to cite this article: Kutlu &, Kutlu FN, Tekin Y. Chronic anogenital ulceration. Indian Dermatol Online J 2020;11:665-6 |
A 62-year-old woman presented with an ulcerative lesion on the anogenital region. The lesion had appeared 4 years ago and had progressively increased in size. She had applied to several hospitals with the complaint of ulcerated lesions. During this period, she had received topical moisturizers, isoconazole nitrate and diflucortolone valerate treatments with the preliminary diagnosis of candidiasis and contact dermatitis. Although the complaint of itching was reduced after previous topical treatments, the patient applied to our clinic due to enlargement of the ulcer. The family history of the patient and physical examination were unremarkable. Dermatological examination revealed a 3.5-cm ulcerated lesion covered with a white pseudomembrane at the inferior of the vulva [Figure 1]. Routine laboratory examinations including complete blood count, urinalysis, biochemical profile, VDRL, HIV, and hepatitis serologies were all within normal limits. Histopathological examination revealed atypical basal cell islands in the dermis. These cell islands were stained strongly positive with Ber-EP4 [Figure 2] and [Figure 3]. | Figure 1: A 3.5-cm ulcerated lesion covered with white pseudomembrane at the inferior of the vulva
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 | Figure 2: Atypical basal cell islands in dermis (Hematoxylin and Eosin, ×200)
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 | Figure 3: The tumor cells were stained strongly positive with Ber-EP4 stain (Ber-EP4, ×200)
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Question | |  |
What is your diagnosis?
Answer | |  |
Anogenital basal cell carcinoma.
Discussions | |  |
Basal cell carcinoma is the most common malignant skin tumor that accounts for 75% of non-melanocytic skin tumors. There are 2.8 million new cases of BCC diagnosed annually in the United States and 700,000 new cases each year in Europe.[1] More than 80% of BCC cases are localized in areas exposed to the sun including the head and neck. Anogenital involvement of the BCC is rare and it is approximately 5% of all BCC cases.[2] To date, few reports have been published in the literature on the anogenital involvement of BCC.[2],[3] Malignancies localized in the anogenital region often present with ulcerated lesions that do not respond to palliative therapies. They present with signs of discharge, irritation, and itching. In this case, ulcerative lesion of the patient did not improve with topical treatments for a long time.[4] Dermoscopic features of classical BCC include wheel-like structures, multiple erosions/ulcers, leaf-like structures, as well as some criteria, such as blue-gray dots/globules and arborizing vessels along with shiny white blotches.[5]
Basal cell carcinoma is characterized by uniform cells with round or oval basophilic nuclei, larger and darker than nuclei of epidermal basal keratinocytes, with minimal cytoplasm. Basal cell carcinoma stains positively with cytokeratin that arises from the follicular epithelium. BerEP4 is diffusely present in most BCC cases, while EMA is infrequently positive.[6] Histopathological examination should be performed for long-term, treatment-resistant ulcerated lesions in the anogenital region in order to rule out malignancy. In this observation, it is aimed to raise awareness of dermatologists in terms of BCC located in the anogenital region.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. The patients have given their consent for their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References | |  |
1. | Mohan SV, Chang Anne Lynn S. Advanced basal cell carcinoma: Epidemiology and therapeutic innovations. Curr Dermatol Rep 2014;3:40-5. |
2. | Chinem VP, Miot HA. Epidemiology of basal cell carcinoma. An Bras Dermatol 2011;86:292-305. |
3. | Bulur I, Boyuk E, Saraçoǧlu ZH, Arik D. Perianal basal cell carcinoma. Case Rep Dermatol 2015;7:25-8. |
4. | Swamiappan M. Anogenital pruritus – An overview. J Clin Diagn Res 2016;10:WE01-3. |
5. | Liopyris K, Navarrete-Dechent C, Yélamos O, Marchetti MA, Rabinovitz H, Marghoob AA. Clinical dermoscopic and reflectance confocal microscopy characterization of facial basal cell carcinomas presenting as small white lesions on sun-damaged skin. Br J Dermatol 2019;180:229-30. |
6. | Kyrpychova L, Carr RA, Martinek P, Vanecek T, Perret R, Chottová-Dvořáková M, et al. Basal cell carcinoma with matrical differentiation: Clinicopathologic, immunohistochemical, and molecular biological study of 22 cases. Am J Surg Pathol 2017;41:738-49. |
[Figure 1], [Figure 2], [Figure 3]
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