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Ano-genital Granulomatosis and Crohn’s Disease: A Case Series of Males Presenting with Genital Lymphoedema
Background and Aims Ano-genital granulomatosis is a rare chronic granulomatous condition of the skin that causes lymphoedema of the external genitalia. There is a reported association with Crohn'sExpand
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A limited form of proteus syndrome with bilateral plantar cerebriform collagenomas and varicose veins secondary to a mosaic AKT1 mutation.
IMPORTANCE Proteus syndrome is an extremely rare disorder of mosaic postnatal overgrowth affecting multiple tissues including bone, soft tissue, and skin. It typically manifests in early childhoodExpand
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Rhabdomyomatous mesenchymal hamartoma resembling scleroderma ‘en coup de sabre’: a case report and literature review
with sparing of the umbilicus. Spreading to the trunk and extremities may occur over a period of days but the face, palms and soles are usually unaffected. The pruritic papules may coalesce to formExpand
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Eosinophilic oesophagitis in adults
its expression was diffuse in 63% of the cases (Figure 1B). CD68 was expressed in all but two cases, diffusely in 61% of cases. FXIIIa expression was seen in all but one case, and was diffuse in 71%Expand
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Familial multiple discoid fibromas: unique histological features and therapeutic response to topical rapamycin
Familial multiple discoid fibromas is a rare genodermatosis that bears some resemblance to Birt–Hogg–Dubé syndrome but is not associated with mutations in the folliculin (FLCN) gene or systemicExpand
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Necrobiotic xanthogranuloma treated with lenalidomide
A 78-year-old white woman presented with a 1-year history of multiple skin nodules in the periorbital and temple areas. She had been diagnosed 6 years earlier with monoclonal gammopathy ofExpand
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Lichen planus in a patient treated with pembrolizumab for metastatic malignant melanoma
Pembrolizumab is a programmed death (PD)-1 receptor inhibitor and a first-line treatment for unresectable metastatic melanoma (MM) that is displaying disease progression following treatment withExpand
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Ecthyma gangrenosum without bacteraemia: evidence in favour of a broader definition
Ecthyma gangrenosum (EG) is often defined as a cutaneous manifestation of Pseudomonas aeruginosa septicaemia, typically secondary to neutropenia. There is increasing recognition that a broaderExpand
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Epidermolysis Bullosa Acquisita (Brunsting-Perry Pemphigoid Variant) Localized to the Face and Diagnosed With Antigen Identification Using Skin Deficient in Type VII Collagen.
Brunsting-Perry pemphigoid is defined as an autoimmune vesiculobullous eruption typically localized on the head and neck region with minimal or no mucosal involvement. The disease tends to run aExpand
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Actinic granuloma: a history of photoexacerbation and the importance of a radial ‘three‐zone’ biopsy
Actinic granuloma (AG) is an uncommon granulomatous skin disease, characterized by annular plaques occurring on sun-exposed skin. We report a patient with a history of photoexacerbation, andExpand
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