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Onychomatricoma
SpecialtyDermatology

Onychomatricoma is a cutaneous condition characterized by a distinctive tumor of the nail matrix.[1]

Symptoms include thickness of the nail plate, transverse or longitudinal overcurvature, xanthonychia, and numerous splinter hemorrhages.

The diagnosis of onychomatricoma is made based on clinical features, dermoscopy, and ultrasonography, and is confirmed by its histological features.

Onychomatricoma is treated by surgical excision.

Signs and symptoms[edit]

Thickness of the nail plate, transverse or longitudinal overcurvature, xanthonychia, and numerous splinter hemorrhage are the four main clinical characteristics of onychomatricoma.[2]

Causes[edit]

According to recent research, onychomatricoma patients may have genetic changes, such as chromosomal deletion.[3]

Diagnosis[edit]

In addition to the traditional tetrad symptoms, other diagnostic techniques such dermoscopy, ultrasonography, and histological findings are also used to make the diagnosis.[2]

Hemorrhagic striae, white longitudinal grooves that match the nail plate channels, and perforations in the distal region of the nail plate are all visible during dermoscopy.[4]

A radiological examination reveals no evidence of onychomatricoma-related underlying bone involvement.[5]

An ultrasonographic examination reveals poor blood flow, a hypoechogenic region corresponding to the fingerlike projections, and a hypoechoic tumoral lesion affecting the nail matrix.[6]

The diagnosis of onychomatricoma is confirmed by its unique histological characteristics.[2] Onychomatricoma is a fibroepithelial tumour that has two different regions.[7] The proximal zone, which is defined by deep epithelial invaginations occupied by overlaying ungual protrusions, is situated beneath the posterior nail fold. The distal zone, corresponding to the lunula, is made up of epithelial digitations that grow from the matrix epithelium and puncture the nail plate.[2]

Among the differential diagnoses are osteochondroma, longitudinal melanonychia, fibrokeratoma, onychomycosis, periungual fibroma, squamous cell carcinoma, Bowen's disease, and subungual verruca vulgaris.[8]

Treatment[edit]

Onychomatricoma is treated with surgical excision.[9] To avoid local recurrence, the tumour must be fully removed, including the normal nail matrix close to the lesion.[10]

Epidemiology[edit]

As of 2016 less than 80 cases of onychomatricoma have been reported.[2] The majority of cases of onychomatricoma are middle-aged women, with a peak incidence occurring in the fifth decade of life.[8][11]

See also[edit]

References[edit]

  1. ^ Freedberg, Irwin M.; Eisen, Arthur Z.; Wolff, Klaus; Austen, K. Frank; Goldsmith, Lowell A.; Katz, Stephen I., eds. (2003). Fitzpatrick's Dermatology in General Medicine (6th ed.). McGraw-Hill. p. 667. ISBN 978-0-07-138076-8.
  2. ^ a b c d e Joo, Hong Jin; Kim, Mi Ri; Cho, Baik Kee; Yoo, Gyeol; Park, Hyun Jeong (2016). "Onychomatricoma: A Rare Tumor of Nail Matrix". Annals of Dermatology. 28 (2). Korean Dermatological Association and The Korean Society for Investigative Dermatology: 237–241. doi:10.5021/ad.2016.28.2.237. ISSN 1013-9087. PMC 4828389. PMID 27081273.
  3. ^ Cañueto, Javier; Santos-Briz, Ángel; García, Juan Luis; Robledo, Cristina; Unamuno, Pablo (2011). "Onychomatricoma: Genome-wide analyses of a rare nail matrix tumor". Journal of the American Academy of Dermatology. 64 (3). Elsevier BV: 573–578.e1. doi:10.1016/j.jaad.2009.07.051. ISSN 0190-9622. PMID 20691500.
  4. ^ Richert, B.; André, J. (2011). "L'onychomatricome". Annales de Dermatologie et de Vénéréologie (in French). 138 (1). Elsevier BV: 71–74. doi:10.1016/j.annder.2010.10.027. ISSN 0151-9638. PMID 21276470.
  5. ^ Miteva, Mariya (2011-09-01). "Nail Clipping Diagnosis of Onychomatricoma". Archives of Dermatology. 147 (9). American Medical Association (AMA): 1118. doi:10.1001/archdermatol.2011.240. ISSN 0003-987X. PMID 21931060.
  6. ^ Soto, Rosamary; Wortsman, Ximena; Corredoira, Yamile (2009-12-01). "Onychomatricoma: Clinical and Sonographic Findings". Archives of Dermatology. 145 (12). American Medical Association (AMA): 1461–1462. doi:10.1001/archdermatol.2009.312. ISSN 0003-987X. PMID 20026866.
  7. ^ Perrin, Ch.; Goettmann, S.; Baran, R. (1998). "Onychomatricoma: Clinical and histopathologic findings in 12 cases". Journal of the American Academy of Dermatology. 39 (4). Elsevier BV: 560–564. doi:10.1016/s0190-9622(98)70004-0. ISSN 0190-9622. PMID 9777762.
  8. ^ a b Tavares, Glaysson Tassara; Chiacchio, Nilton Gioia Di; Chiacchio, Nilton Di; Souza, Marcos Vilela de (2015). "Onychomatricoma: a tumor unknown to dermatologists". Anais Brasileiros de Dermatologia. 90 (2). FapUNIFESP (SciELO): 265–267. doi:10.1590/abd1806-4841.20153650. ISSN 0365-0596. PMC 4371682. PMID 25831003.
  9. ^ Estrada-Chavez, Guadalupe; Vega-Memije, M. E.; Toussaint-Caire, S.; Rangel, L.; Dominguez-Cherit, J. (2007). "Giant onychomatricoma: report of two cases with rare clinical presentation". International Journal of Dermatology. 46 (6). Wiley: 634–636. doi:10.1111/j.1365-4632.2007.03300.x. ISSN 0011-9059. PMID 17550569.
  10. ^ Gaertner, Erich M.; Gordon, Michael; Reed, Thomas (2009-09-17). "Onychomatricoma: case report of an unusual subungual tumor with literature review". Journal of Cutaneous Pathology. 36 (s1). Wiley: 66–69. doi:10.1111/j.1600-0560.2008.01218.x. ISSN 0303-6987. PMID 19469867.
  11. ^ Di Chiacchio, N.; Tavares, G.T.; Tosti, A.; Di Chiacchio, N.G.; Di Santis, E.; Alvarenga, L.; Stuhr, P.; De Farias, D. (2015-08-27). "Onychomatricoma: epidemiological and clinical findings in a large series of 30 cases". British Journal of Dermatology. 173 (5). Oxford University Press (OUP): 1305–1307. doi:10.1111/bjd.13900. ISSN 0007-0963. PMID 25970230.

Further reading[edit]

External links[edit]

source: https://en.wikipedia.org/wiki/Onychomatricoma

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