Anogenital Crohn’s Disease and Granulomatosis: A Systematic Review of Epidemiology, Clinical Manifestations, and Treatment

Author:

Honap Sailish12,Meade Susanna1,Spencer Ashley3,Pavlidis Polychronis12,Luber Raphael P1,Calonje Eduardo4,Rashidghamat Ellie5,Bunker Christopher B6,Lewis Fiona5,Irving Peter M12

Affiliation:

1. IBD Centre, Guy’s and St Thomas’ NHS Foundation Trust, London, UK

2. School of Immunology and Microbial Sciences, King’s College London, London, UK

3. Department of Dermatology, Hammersmith Hospital, Imperial College Healthcare NHS Trust, London, UK

4. Department of Dermatopathology, St John’s Institute of Dermatology, Guy’s and St. Thomas’ NHS Foundation Trust, London, UK

5. Department of Dermatology, St John’s Institute of Dermatology, Guy’s and St Thomas’ NHS Foundation Trust, London, UK

6. Dermatology Department, University College London Hospitals NHS Foundation Trust, London, UK

Abstract

Abstract Background and Aims Metastatic Crohn’s disease is an extraintestinal cutaneous manifestation characterised by non-specific inflammatory lesions anatomically separate from the gut; genital involvement is rare. We conducted a systematic review of anogenital Crohn’s disease and granulomatosis, to provide a synthesis of epidemiology, clinical features, and treatment outcomes. Methods A systematic search of the literature was conducted via MEDLINE, EMBASE, and the Cochrane database from inception to December 1, 2020. Two investigators extracted and analysed study data. Response and remission were defined as partial improvement or complete resolution of symptoms and examination findings, respectively. Results Of 9381 screened studies, 185 articles, [410 cases: 273 female, 137 male] were included. The predominant clinical features were oedema, ulcers, fissures, and hypertrophic lesions. Adults and children present similarly. Luminal Crohn’s disease was diagnosed in nearly 80% of cases including 45–80% patients without gastrointestinal symptoms (time to inflammatory bowel disease [IBD] from anogenital Crohn’s disease diagnosis [range] –43 to 11 years). Antibiotics, corticosteroids, thiopurines, and anti-tumour necrosis factor [TNF] therapy were the most frequently prescribed agents. At final follow-up, non-response, response, and remission rates were 37/304 [12%], 267/304 [88%], and 114/304 [38%], respectively. Oedema was associated with a poor response to topical therapy. Greater response rates to anti-TNF therapy were seen in patients prescribed concomitant immunomodulation [24/25, 96% vs 67/90, 74%, p = 0.02]. Conclusions We provide an illustrative summary of the clinical presentation and treatment effectiveness of this rare, under-recognised condition, and a proposed algorithm for approach and management. Prospective studies with longer follow-up are required to define optimal treatment strategies.

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

Reference26 articles.

1. Extraintestinal manifestations of idiopathic inflammatory bowel disease;Danzi;Arch Intern Med,1988

2. Cutaneous manifestations of gastrointestinal disease: part II;Thrash;J Am Acad Dermatol,2013

3. Crohn’s disease with cutaneous involvement;Parks;Proc R Soc Med,1965

4. Cutaneous ulceration in Crohn’s disease;Mountain;Gut,1970

5. Ano-genital granulomatosis: the counterpart of oro-facial granulomatosis;Scheur;J Eur Acad Dermatol Venereol,2003

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