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2023, Number 2

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Dermatología Cosmética, Médica y Quirúrgica 2023; 21 (2)

Congenital tufted angioma. A case report

Arteaga PR, Guerrero HDV, Infante FC, Toussaint CS, Vega MME

Language: Spanish
References: 18
Page: 126-129
PDF size: 170.96 Kb.


ABSTRACT

Congenital tufted angioma is a benign vascular neoformation with a rare presentation in childhood that can involve skin, subcutaneous cell tissue, and even fascia and muscle. Mutations of the nras and gna14 genes have been associated and a wide range of clinical presentations The most common is an indurated erythematous-violaceous plaque with a vascular appearance that may be associated with local pain and hair growth or sweating. In most cases, it usually regresses, leaving an area of atrophy on the affected skin; however, various treatments have been described, including topical steroids. We report the case of a 5-month-old female with a plaque-type neoformation on the left shoulder with a histological diagnosis of tufted angioma with improvement of the dermatosis and mobility after treatment.


REFERENCES

  1. pdq Pediatric Treatment Editorial Board, Childhood vasculartumors treatment (pdq®): health professional version. En pdqcancer information summaries, National Cancer Institute (EstadosUnidos), 2022. Disponible en: https://www.ncbi.nlm.nih.gov/books/NBK343452/#CDR0000774170__3.

  2. Da Silva CM, Schettini APM, Santos M y Chirano CAR, Tuftedangioma, An Bras Dermatol 2017; 92:742.3. Disponible en:https://doi.org/10.1590/abd1806-4841.20175896.

  3. Ten Broek RW, Koelsche C, Eijkelenboom A, Mentzel T, CreytensD, Vokuhl C et al., Kaposiform hemangioendothelioma andtufted angioma: (epi)genetic analysis including genome-widemethylation profiling, Ann Diagn Pathol 2020; 44:151434. Disponibleen: https://doi.org/10.1016/j.anndiagpath.2019.151434.

  4. Martínez AV, Sánchez LC, Martínez AE, Cubells JE, Bosch IF, DeMiquel VA et al., Angiomas en penacho en la infancia. Serie de9 casos y revisión de la literatura, An Pediatr 2015; 83:201-8. doi:10.1016/j.anpedi.2014.10.018.

  5. Wang L, Liu L, Wang G y Gao T, Congenital disseminated tuftedangioma, J Cutan Pathol 2013; 40:405-8. Disponible en: https://doi.org/10.1111/cup.12089.

  6. Rambhia KD y Khopkar US, Tufted angioma, Indian Dermatol OnlineJ 2016; 7:62-3. Disponible en: https://doi.org/10.4103/2229-5178.174313.

  7. Putra J y Al-Ibraheemi A, Vascular anomalies of the head andneck: a pediatric overview, Head Neck Pathol 2021; 15:59-70.Disponible en: https://doi.org/10.1007/s12105-020-01236-x.

  8. Johnson EF, Davis DM, Tollefson MM, Fritchie K y Gibson LE,Vascular tumors in infants: case report and review of clinical,histopathologic, and immunohistochemical characteristics ofinfantile hemangioma, pyogenic granuloma, non-involutingcongenital hemangioma, tufted angioma, and kaposiform hemangioendothelioma,Am J Dermatopathol 2018; 40:231-9. Disponibleen: https://doi.org/10.1097/dad.0000000000000983.

  9. Mehrotra K, Khunger N, Sharma S, Muradia I, Chakravarty P yKathuria S, Tufted angioma with coagulopathy: a dermoscopicevaluation and successful treatment, Int J Dermatol 2021;60:e379-81. Disponible en: https://doi.org/10.1111/ijd.15593.CLARIZA INFANTE FERNÁNDEZ Y COLS. ANGIOMA EN PENACHO CONGÉNITO

  10. Lim YH, Fraile C, Antaya RJ y Choate KA, Tufted angioma withassociated Kasabach-Merritt phenomenon caused by somaticmutation in gna 14, Pediatr Dermatol 2019; 36:963-4.

  11. Browning J, Frieden I, Baselga E, Wagner A y Metry D, Congenital,self-regressing tufted angioma, Arch Dermatol 2006;142:749-51. Disponible en: https://doi.org/10.1001/archderm.142.6.749.

  12. Feito-Rodríguez M, Sánchez-Orta A, De Lucas R, López-GutiérrezJC, Ruiz-Bravo E, Baselga E et al., Congenital tufted angioma:a multicenter retrospective study of 30 cases, Pediatr Dermatol2018; 35:808-16. Disponible en: https://doi.org/10.1111/pde.13683.

  13. Escudero-Góngora MM, Corral-Magaña O, Gómez C y Martín-Santiago A, Topical rapamycin: an additional therapeuticoption for tufted angioma in adults, Actas Dermosifiliogr2018; 109:192-4. Disponible en: https://doi.org/10.1016/j.ad.2017.04.026.

  14. Mariani LG, Schmitt IR, García CD y Kiszewski AE, Low dose sirolimustreatment for refractory tufted angioma and congenitalkaposiform hemangioendothelioma, both with Kasabach‐Merrittphenomenon, Pediatr Blood Cancer 2019; 66:e27810. Disponibleen: https://doi.org/10.1002/pbc.27810.

  15. Ragab IA, Abdel-Kader SM, Abou Zeid AA, Mohammad SA,Abdel Raheem HG y Aly NH, A successful tale of sirolimustreatment in refractory vascular tumors, J Pediatr Surg CaseRep 2022; 78:102180. Disponible en: https://doi.org/10.1016/j.epsc.2022.102180.

  16. Pfister BK, King EC, Samet JD, Gulliver J y Wolf SF., Tufted angiomaof the index finger middle phalanx, J Am Acad Orthop SurgGlob Res Rev 2022; 6. Disponible en: https://doi.org/10.5435/JAAOSGlobal-D-21-00301.

  17. Behera B, Remya R, Chandrashekar L, Thappa DM y GochhaitD, Tufted angioma successfully treated with topical timololgel-forming solution, Indian J Dermatol Venereol Leprol 2021;87(4):581-4. doi: 10.25259/IJDVL_822_20.

  18. Xiao Y, Hao D, Li Y, Ji Y y Jiang X, Topical tacrolimus reduces thesevere pain of tufted angioma: case report, Dermatol Ther 2020;33:e14412. Disponible en: https://doi.org/10.1111/dth.14412.




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