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Case Reports
. 2024 Apr 17;17(4):e257572.
doi: 10.1136/bcr-2023-257572.

Aplasia cutis congenita type VII of the lower extremity: a favourable disease course with minimal conservative treatment

Affiliations
Case Reports

Aplasia cutis congenita type VII of the lower extremity: a favourable disease course with minimal conservative treatment

Kwong Tack Quach et al. BMJ Case Rep. .

Abstract

Aplasia cutis congenita (ACC) is a group of rare heterogeneous disorders characterised by absent areas of skin at birth. The majority of cases involve the scalp region. ACC limited to one lower limb is extremely rare. We report an usual case of ACC limited to the left thigh of which healing occurred in utero. The case was managed conservatively and the disease course has been favourable with no limitations in limb function and an entirely normal development. Most cases of ACC are self-healing, justifying a conservative approach. This holds further true for ACC limited to one lower limb where the majority of cases reported to date show a favourable disease course with minimal conservative treatment.

Keywords: Dermatological; Dermatology; Medical management; Skin.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
(A) Clinical features on the day of birth: a well-demarcated gyriform-shaped erythematous atrophic plaque of 1.5 by 2 cm with central purple discolouration on the lateral side of the left thigh. (B) Dermatoscopic features on the day of birth: erythema and white streaks centrally with telangiectasia at the border.
Figure 2
Figure 2
(A) Clinical features 3 months after birth. (B) Dermatoscopic features 3 months after birth.

References

    1. Frieden IJ. Aplasia cutis congenita: a clinical review and proposal for classification. J Am Acad Dermatol 1986;14:646–60. 10.1016/s0190-9622(86)70082-0 - DOI - PubMed
    1. Coi A, Barisic I, Garne E, et al. . Epidemiology of aplasia cutis congenita: a population‐based study in Europe. Acad Dermatol Venereol 2023;37:581–9. 10.1111/jdv.18690 - DOI - PubMed
    1. Ahčan U, Janeič T. Management of aplasia cutis congenita in a non-scalp location. British Journal of Plastic Surgery 2002;55:530–2. 10.1054/bjps.2002.3915 - DOI - PubMed
    1. Bigliardi PL, Braschler C, Kuhn P, et al. . Unilateral aplasia cutis congenita on the leg. Pediatr Dermatol 2004;21:454–7. 10.1111/j.0736-8046.2004.21406.x - DOI - PubMed
    1. Lee JS, Yun SJ, Lee JB, et al. . A case of aplasia cutis congenita, type VII. Ann Dermatol 2008;20:70–3. 10.5021/ad.2008.20.2.70 - DOI - PMC - PubMed

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