• Nenhum resultado encontrado

Rev. Bras. . vol.74 número4 en a27v74n4

N/A
N/A
Protected

Academic year: 2018

Share "Rev. Bras. . vol.74 número4 en a27v74n4"

Copied!
1
0
0

Texto

(1)

637

BRAZILIAN JOURNAL OFOTORHINOLARYNGOLOGY 74 (4) JULY/AUGUST 2008

http://www.rborl.org.br / e-mail: revista@aborlccf.org.br CASE REPORT

Solitary nasal

trichoepithelioma

Lucas Gomes Patrocinio1, Priscila Garcia Damasceno2, Tomas Gomes Patrocinio3, José Antonio Patrocinio4

INTRODUCTION

Trichoepitheliomas are benign cuta-neous neoplasms occurring mostly on the face, which derive from pillous follicles.1

There are two clinical presentations: a here-ditary sex-linked multiple form that usually affects the face, scalp and upper thorax of young adults; and a non-hereditary solitary form that may affect any part of the body (but mostly the face) of adults.1 The

dia-meter is rarely more than 2 to 3 cm.2 It is an extremely rare tumor; in the literature we surveyed, there were only two cases of trichoepitheliomas involving the skin in the nose area.3,4

This paper reports a case of a soli-tary nasal trichoepithelioma that was remo-ved surgically, followed by a flap rotation. We discuss the diagnostic and therapeutic aspects of this rare skin tumor.

CASE REPORT

JCM, a male patient aged 56 years, complained of a slow-growing lesion on the dorsum of the nose during the past five years. The physical examination showed a brownish nodule on the dorsum of the nose, with visible blood vessels, a fibroe-lastic consistency, and measuring 3.0 x 2.5 cm (Figure 1A). The initial diagnosis was a basocellular carcinoma. The nodule was resected surgically (Figure 1B) and sent to the pathology department, which described islands of basaloid cells within small cystic structures filled with laminated keratin and epithelial cells to form invaginations similar to follicular papillae. A diagnosis of

trichoepithelioma was confirmed and the tumor was shown to have free margins. A nasogenian flap was used for reconstruc-ting the nose (Figures 1C and 1D). The patient was monitored for 48 months with no recurrences.

DISCUSSION

Solitary trichoepitheliomas are non-hereditary benign trichogenic tumors of very low incidence that affect adults.2

We found only two cases of solitary nasal trichoepitheliomas in the literature.3,4

The multiple and solitary forms are morphologically identical; they may be differentiated by the number of lesions2,3

These tumors are firm, translucent nodules or papules.5

The differential diagnosis of the solitary form is made mostly with the

basocellular carcinoma, but also with the trichofoliculoma, melanocytic nevi and sebaceous hyperplasia. Histopathology provides the final diagnosis.1

Histologically, it is a well-differen-tiated tumor containing hair-forming struc-tures and keratinous cysts surrounded by basophilic cells in an adenoid pattern.5

Generally, surgical removal of the lesion for pathology is curative. In 1999, Jemec et al.5 reviewed the first ten cases

of the literature and found a recurrence in only one case after surgical removal.

FINAL COMMENTS

Solitary trichoepitheliomas are extremely rare benign tumors that should be considered when finding a single solid nodule or papula on the face. Confirma-tion by excision biopsy is essential for the diagnosis and treatment.

REFERENCES

1.Boni R, Fogt F, Vortmeyer AO, Tronic BS, Zhuang Z. Genetic analysis of a trichoepi-thelioma and associated basal cell carcinoma. Arch Dermatol 1998;134(9):1170-1. 2.Filho GB, Toppa NH, Miranda D, Matos MP,

Silva AL. Giant solitary trichoepithelioma. Arch Dermatol 1984;120:797-8.

3.Dvir E. Solitary trichoepithelioma in a 70-year-old man. Arch Dermatol 1981;117:455-6. 4.Riberti C, Vaienti L, Parodi PC, Azzolini C. [A

nasal reconstruction via the expansion of the tissue] [Article in Italian]. Acta Otorhinolaryn-gol Ital 1993;13(5):407-22.

5.Jemec B, Lovgreen Nielsen P, Jemec GB, Balsev E. Giant solitary trichoepithelioma. Dermatol Online J 1999;5(1):1.

Keywords: plastic surgery, skin neoplasms, nasal neoplasms.

1 Otorhinolaryngologist, physician of the Otorhinolaryngology Unit, Medical School of the Universidade Federal de Uberlandia. 2 Physician, resident of the Otorhinolaryngology Unit, Medical School of the Universidade Federal de Uberlandia. 3 Physician, resident of the Otorhinolaryngology Unit, Medical School of the Universidade Federal de Uberlandia. 4 Professor Titular, Chefe of the Otorhinolaryngology Unit, Medical School of the Universidade Federal de Uberlandia.

Otorhinolaryngology Unit, Medical School of the Universidade Federal de Uberlandia, Minas Gerais, Brasil. Address for correspondence: Lucas Gomes Patrocinio - Rua Arthur Bernardes 555 1o. andar Uberlandia MG 38.400-368.

Tel/Fax: (0xx34) 3215-1143 - E-mail: lucaspatrocinio@triang.com.br

This paper was submitted to the RBORL-SGP (Publishing Manager System) on 17 November 2006. code 3522. The article was accepted on 20 January 2007.

Rev Bras Otorrinolaringol 2008;74(4):637.

Imagem

Figure 1. Pictures showing a solitary nasal trichoepithelioma (A)  removed surgically (B) and after reconstruction with a nasogenian  flap (C e D).

Referências

Documentos relacionados

O trabalho artístico realizado em contextos prisionais - os atores sociais em interação sobre o seu território (a instituição total) - as relações entre os grupos de reclusos e

Depois se simula o comportamento energético de uma microrrede que inclui estas tecnologiasconectadas à rede elétrica principal com sistema de compensação de energia ou

Therefore, in order to know if is also translated in this life cycle stage, the expression of HoMu::GFP was compared with the expression of DOZI, CITH, Puf2, 4E and wild type

Malignancy associated with splenogonadal fusion is exceedingly rare and, to our knowledge, only three cases of this association have been reported in the literature (3) .We report

Hibernoma is a rare benign adipose tumor composed of brown fat cells and only about ten cases occurring in the cervical area have been reported.. We reported two rare cases

Primary sarcoma of the penis is a very rare condition, and to date there are only around 44 cases described in the medical literature, of which 30 are leiomyosarcomas

The cerebral or cerebellar tu- moral form of schistosomiasis mansoni is extremely rare, there are only 12 cases prior related 1-5,7-10.. We describe a curious case in which Manson’s

phy of the basal ganglia and cerebellum (H-ABC) is a nosologic entity described in 2002, by van der Knaap and coworkers 2.. It is an extremely