Atrophia maculosa varioliformis cutis

Atrophia Maculosa Varioliformis Cutis (AMVC) is an idiopathic noninflammatory macular atrophy subtype that affects young people. Clinically, it is distinguished by a variety of shaped, shallow, sharply demaracated depressions.[1]

Atrophia maculosa varioliformis cutis
SpecialtyDermatology

Signs and symptoms

edit

The clinical feature of AMVC is the spontaneous onset of atrophic lesions that are usually on the face of adolescents. These lesions can be round, oval, linear, curvilinear, or rectangular with a regular margin and clearly defined edges. The sites most commonly affected are the bilateral malar regions. However the mandibular region and forehead may also be impacted. The absence of prior inflammatory or traumatic events at the lesion site is characteristic of this condition.[2] There have been reports of extrafacial involvement, such as lesions on the forearm, posterior aspect of the pinna, and periumbilical area.[3][4] The lesion may range in size from 0.2-2 cm in length and 0.2-0.5 cm in width; neither exfoliation nor pigmentary changes may be present. They are cicatricial and depressed in comparison to the surrounding skin.[2]

Causes

edit

Although the exact cause of AMVC is unknown, a familial occurrence that has been documented in the past raises the possibility that the condition is inherited rather than the result of an environmental insult.[5][3] There have been reports of cases linked to pachydermodactyly and extrahepatic biliary atresia, although these links might be accidental.[6][7]

Diagnosis

edit

Patients with facial atrophic lesions with well-defined edges and no erythema, induration, pigmentary changes, or honeycombed pattern are typically diagnosed with AMVC primarily based on clinical findings. With a comparatively normal dermis, a small reduction in or fragmentation of the elastic fibers, no fibrosis, and little to no inflammation beneath the shallow depression of the epidermis, the histological features are nonspecific.[8]

References

edit
  1. ^ Kim, En Hyung; Kang, Hee Young (2008). "A Case of Atrophia Maculosa Varioliformis Cutis". Annals of Dermatology. 20 (4). XMLink: 244–246. doi:10.5021/ad.2008.20.4.244. ISSN 1013-9087. PMC 4903990. PMID 27303203.
  2. ^ a b Sethy, Mitanjali; Sachan, Suvigya; Srinivas, ChakravarthiR; Sahu, Satyajit (2021). "Atrophia maculosa varioliformis cutis: A rare case report". Indian Dermatology Online Journal. 12 (2). Medknow: 346–348. doi:10.4103/idoj.idoj_270_20. ISSN 2229-5178. PMC 8088183. PMID 33959542.
  3. ^ a b Gordon, P.M.; Doherty, V.R. (1996). "Familial atrophia maculosa varioliformis cutis". British Journal of Dermatology. 134 (5). Oxford University Press (OUP): 982–983. doi:10.1111/j.1365-2133.1996.tb06345.x. ISSN 0007-0963. PMID 8736355. S2CID 1850815.
  4. ^ Criado, PR; Pegas, JR; Tebecherani, A; Souza, AC; Sueto, M; Pires, MC (May 5, 2005). "Atrophia maculosa varioliformis cutis: a case with extrafacial involvement and familial facial lesions". Journal of the European Academy of Dermatology and Venereology. 19 (6). Wiley: 764–766. doi:10.1111/j.1468-3083.2005.01251.x. ISSN 0926-9959. PMID 16268891. S2CID 7485371.
  5. ^ MARKS, V.J.; MILLER, O.F. (1986). "Atrophia maculosa varioliformis cutis". British Journal of Dermatology. 115 (1). Oxford University Press (OUP): 105–109. doi:10.1111/j.1365-2133.1986.tb06227.x. ISSN 0007-0963. PMID 3730277. S2CID 45573880.
  6. ^ Venencie, Pierre Y.; Foldès, Christine; Cuny, Michèle; Samuel, Didier; Bismuth, Henri (1989). "Atrophia maculosa varioliformis cutis with extrahepatic biliary atresia". Journal of the American Academy of Dermatology. 21 (2). Elsevier BV: 309. doi:10.1016/s0190-9622(89)70185-7. ISSN 0190-9622. PMID 2768583.
  7. ^ Callot, V.; Wechsler, J.; Hovnanian, A.; Revuz, J. (1995). "Pachydermodactyly and Atrophia maculosa varioliformis cutis". Dermatology. 190 (1). S. Karger AG: 56–58. doi:10.1159/000246636. ISSN 1018-8665. PMID 7894099.
  8. ^ Nakayama, H; Mihara, M (May 1, 1995). "Atrophia maculosa varioliformis cutis". Acta Dermato-Venereologica. 75 (3). Medical Journals Sweden AB: 252. doi:10.2340/0001555575252. ISSN 1651-2057. PMID 7653197.

Further reading

edit
edit