Syndrome du Morbihan et furosémide

Valois, A.; Demarez, B.; Abed, S.; Fouet, B.; Boyé, T.; Morand, Jean‐Jacques

doi:10.1016/j.annder.2019.09.345

Cited by 1 publication

(2 citation statements)

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“…This is a 39-year-old patient with no notable pathological history. His history of the disease goes metronidazole Ketotifen, Triamcinolone injection, Retinoids, thalidomide [9], Omalizumab [3], Diuretics [5]. Blepharoplasty by CO2 laser [10], Reduction surgery [11], some authors recommend combined treatments [12].…”

Section: Observationmentioning

confidence: 99%

“…Indeed, this edema could be secondary to the permanent obstruction of the dermal lymphatics by mast cells or linked to dermal fibrosis induced by these cells [4]. Clinically, chronic erythematous asymmetric edema of the upper two thirds of the face generally affects the forehead, glabella, eyelids, nose, and cheeks, associated with telangiectasia, facial redness, papules, pustules, nodules [5]. It poses a problem of differential diagnosis mainly with chronic lupus erythematosus, Merkelson-Rosenthal syndrome in its atypical form, dermatomyositis [6].…”

Section: Source Of Supportmentioning

confidence: 99%

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Morbihan Disease: About a Case

Hamraoui,

Soughi,

Baybaye

et al. 2024

Clin Med Rev Case Rep

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Morbihan disease (MD) is a rare entity. Its nosography is poorly understood, and its therapeutic management is difficult. We report a new case of MD. We report the case of a 39-year-old patient consulted in our department for a year with facial edema, erythema and papules reported by him, for which the patient was treated with cyclines, local and general corticosteroid therapy, without improvement. Clinical examination reveals significant edema of the forehead and eyelids with erythema of the cheeks covered with some telangiectasia. Clinical, biological, and histological findings lead to the diagnosis of Morbihan disease after exclusion of other diseases. Due to previous treatment failures, the patient was placed on duiretics with slight improvement. The particularity of our observation lies in the rarity and especially in the therapeutic difficulties encountered during this disease.

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