The clinical syndrome characterized by an acute mucositis, with variable involvement of the oral, ocular, and genital mucosa and minimal or absent skin involvement, has been described as “atypical Stevens-Johnson syndrome,” “Stevens-Johnson syndrome without skin lesions,” and “Fuchs syndrome.” In the past few years, a new nomenclature was introduced, mostly focused on the etiologic agent, Mycoplasma pneumoniae, including terms such as “Mycoplasma pneumoniae–associated mucositis”1,2 and “Mycoplasma-induced rash and mucositis”3; more recently, the concept of reactive infectious mucocutaneous eruption (RIME) has been proposed to act as an umbrella term including all mucosa-predominant acute parainfectious eruptions.
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Vassallo et al. (2021) studied this question.
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