Mycoplasma pneumoniae-associated Mucositis: A Recently Described Entity

Mycoplasma pneumoniae (MP) is a common cause of respiratory infections and can be associated with extrapulmonary complications. MP mucositis has recently been described as a distinct endemic clinical entity called Mycoplasma pneumoniae-induced rash and mucositis (MIRM). The authors present the case...

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Main Authors: Inês Zão, Fani Ribeiro, Valter Rocha, Pedro Neto, Carla Matias, Gorete Jesus
Format: Article
Language:English
Published: SMC MEDIA SRL 2018-11-01
Series:European Journal of Case Reports in Internal Medicine
Subjects:
Online Access:https://www.ejcrim.com/index.php/EJCRIM/article/view/977
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spelling doaj-0afa1567566a4ddeab341dcbcfc92f5a2020-11-25T00:45:00ZengSMC MEDIA SRLEuropean Journal of Case Reports in Internal Medicine2284-25942018-11-0151110.12890/2018_000977977Mycoplasma pneumoniae-associated Mucositis: A Recently Described EntityInês Zão0Fani Ribeiro1Valter Rocha2Pedro Neto3Carla Matias4Gorete Jesus5Internal Medicine Department, Centro Hospitalar do Baixo Vouga, Aveiro, PortugalInternal Medicine Department, Centro Hospitalar do Baixo Vouga, Aveiro, PortugalIntensive Care Department, Centro Hospitalar Entre Douro e Vouga, Santa Maria da Feira, PortugalInternal Medicine Department, Centro Hospitalar do Baixo Vouga, Aveiro, PortugalInternal Medicine Department, Centro Hospitalar do Baixo Vouga, Aveiro, PortugalInternal Medicine Department, Centro Hospitalar do Baixo Vouga, Aveiro, PortugalMycoplasma pneumoniae (MP) is a common cause of respiratory infections and can be associated with extrapulmonary complications. MP mucositis has recently been described as a distinct endemic clinical entity called Mycoplasma pneumoniae-induced rash and mucositis (MIRM). The authors present the case of a 46-year-old man with atypical pneumonia associated with exuberant mucositis, conjunctival hyperaemia and positive serological assays for MP IgM. The patient was treated with azithromycin and systemic corticosteroid therapy. Supportive care including pain management, intravenous hydration and mucosal care was also given. There was complete resolution of the pneumonia and mucositis. The presence of atypical pneumonia with mucosal involvement without cutaneous lesions and a favourable clinical evolution led to the diagnosis of MIRM.https://www.ejcrim.com/index.php/EJCRIM/article/view/977Mycoplasma pneumoniaemucositisconjunctival hyperaemiaatypical pneumonia
collection DOAJ
language English
format Article
sources DOAJ
author Inês Zão
Fani Ribeiro
Valter Rocha
Pedro Neto
Carla Matias
Gorete Jesus
spellingShingle Inês Zão
Fani Ribeiro
Valter Rocha
Pedro Neto
Carla Matias
Gorete Jesus
Mycoplasma pneumoniae-associated Mucositis: A Recently Described Entity
European Journal of Case Reports in Internal Medicine
Mycoplasma pneumoniae
mucositis
conjunctival hyperaemia
atypical pneumonia
author_facet Inês Zão
Fani Ribeiro
Valter Rocha
Pedro Neto
Carla Matias
Gorete Jesus
author_sort Inês Zão
title Mycoplasma pneumoniae-associated Mucositis: A Recently Described Entity
title_short Mycoplasma pneumoniae-associated Mucositis: A Recently Described Entity
title_full Mycoplasma pneumoniae-associated Mucositis: A Recently Described Entity
title_fullStr Mycoplasma pneumoniae-associated Mucositis: A Recently Described Entity
title_full_unstemmed Mycoplasma pneumoniae-associated Mucositis: A Recently Described Entity
title_sort mycoplasma pneumoniae-associated mucositis: a recently described entity
publisher SMC MEDIA SRL
series European Journal of Case Reports in Internal Medicine
issn 2284-2594
publishDate 2018-11-01
description Mycoplasma pneumoniae (MP) is a common cause of respiratory infections and can be associated with extrapulmonary complications. MP mucositis has recently been described as a distinct endemic clinical entity called Mycoplasma pneumoniae-induced rash and mucositis (MIRM). The authors present the case of a 46-year-old man with atypical pneumonia associated with exuberant mucositis, conjunctival hyperaemia and positive serological assays for MP IgM. The patient was treated with azithromycin and systemic corticosteroid therapy. Supportive care including pain management, intravenous hydration and mucosal care was also given. There was complete resolution of the pneumonia and mucositis. The presence of atypical pneumonia with mucosal involvement without cutaneous lesions and a favourable clinical evolution led to the diagnosis of MIRM.
topic Mycoplasma pneumoniae
mucositis
conjunctival hyperaemia
atypical pneumonia
url https://www.ejcrim.com/index.php/EJCRIM/article/view/977
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AT pedroneto mycoplasmapneumoniaeassociatedmucositisarecentlydescribedentity
AT carlamatias mycoplasmapneumoniaeassociatedmucositisarecentlydescribedentity
AT goretejesus mycoplasmapneumoniaeassociatedmucositisarecentlydescribedentity
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