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Paeds Vivasnephrology-urology-fluids-and-electrolytes

Paeds Vivas · nephrology-urology-fluids-and-electrolytes

Vulvovaginal and common prepubertal gynaecological disorders: Viva

Branching clinical structured oral on the common prepubertal gynaecological disorders covering the classification and management of vulvovaginitis, the conservative approach to labial adhesions, the corticosteroid treatment of lichen sclerosus, and the red flags of foreign body and sexual abuse.

branching clinical structured oral3 min readVerification in progress

Target exams

RACP DWERACP DCEMRCPCH Clinical
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Target exams

RACP DWERACP DCEMRCPCH Clinical
Prompt
A 5-year-old girl presents with a 2-month history of intense vulval itching and soreness. Her mother has noticed small white patches on the vulval skin. The girl is otherwise well and has no urinary symptoms. On examination there are porcelain-white, atrophic, wrinkled plaques in a figure-of-eight distribution around the vulva and the anus, with a few small purpuric spots. The examiner asks how you would confirm the diagnosis, what the management is, and how your answer would change if the findings included bruising and behavioural concerns.

Branch 1: Confirming the diagnosis

The candidate should recognise the presentation as classic paediatric lichen sclerosus, a chronic inflammatory dermatosis of unknown cause that presents with intense pruritus, soreness, and the characteristic porcelain-white, atrophic, wrinkled plaques in the figure-of-eight distribution around the vulva and the anus. [8] The small purpuric spots are typical of the active disease, in which the fragile sclerotic skin bruises and tears with minimal trauma. The diagnosis is clinical in the great majority of cases and rests on the recognition of this distribution and this appearance. [10]

If the examiner presses on the differential diagnosis, the candidate must distinguish lichen sclerosus from vulval vitiligo, which is depigmented but not atrophic or pruritic, from atopic or contact dermatitis, which is erythematous and itchy but lacks the porcelain-white sclerosis, and from the bruising and scarring of sexual abuse. [10] A skin biopsy confirming the epidermal atrophy, the basement membrane thickening, the upper dermal collagen homogenisation, and the band of lymphocytic inflammation is reserved for cases where the diagnosis is uncertain or the condition does not respond to an appropriate course of treatment. [9]

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References4ShowHide
  1. [8]Bercaw-Pratt JL, Boardman LA, Simms-Cendan JS Clinical recommendation: pediatric lichen sclerosus. J Pediatr Adolesc Gynecol, 2014.PMID 24602304
  2. [9]De Luca DA, Papara C, Vorobyev A Lichen sclerosus: The 2023 update. Front Med (Lausanne), 2023.PMID 36873861
  3. [10]Fistarol SK, Itin PH Diagnosis and treatment of lichen sclerosus: an update. Am J Clin Dermatol, 2013.PMID 23329078
  4. [11]Kirtschig G, Kinberger M, Kreuter A EuroGuiderm guideline on lichen sclerosus-Treatment of lichen sclerosus. J Eur Acad Dermatol Venereol, 2024.PMID 38822598
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