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Updated: Jan 10, 2026

Antigen-Capture Enzyme-Linked Immunosorbent Assay for Specific Detection of Mycoplasma pneumoniae
Published on: February 24, 2023
Mycoplasma pneumoniae-Induced Rash and Mucositis: Clinicopathologic Characterization of 11 Cases
Margaret Lang Houser1, Jennifer B Mancuso1, Johann E Gudjonsson1
1Department of Dermatology, University of Michigan, Ann Arbor, Michigan, USA.
Background:
Mycoplasma pneumoniae -induced rash and mucositis (MIRM) is a mucocutaneous eruption affecting children and young adults with respiratory tract or clinically occult infection by M. pneumoniae . Mucosal involvement is often robust and may raise concern for Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN). Histopathologic changes in MIRM have not been systematically evaluated.
Methods:
Eleven cases of clinically and serologically confirmed MIRM with biopsies available were included in this study. Clinical and histopathologic features were reviewed and recorded.
Results:
All cases displayed a vacuolar to lichenoid interface reaction with apoptotic keratinocytes or cytoid bodies confined to the epidermis. Subepithelial split and epithelial necrosis were observed in about half of the cases, some of which closely mimicked SJS/TEN histopathologically. There was a predominance of neutrophils over lymphocytes in the lichenoid infiltrate in a small subset of cases, a finding that was associated with leukocytosis and concomitant disease involvement of skin and all three mucosal sites.
Conclusions:
The majority of MIRM cases demonstrated histopathologic features indistinguishable from those of erythema multiforme or SJS/TEN, with the exception of a neutrophil-rich lichenoid infiltrate observed in a small subset of cases. MIRM is essentially synonymous with erythema multiforme major associated with M. pneumoniae infection. Correlation with clinical and serologic findings is necessary to exclude SJS/TEN.
Insights
Mycoplasma pneumoniae-induced rash and mucositis (MIRM) presents with skin and mucosal lesions. Histopathology often mimics Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN), necessitating clinical correlation.
Area of Science:
- Dermatology
- Infectious Diseases
- Pathology
Background:
- Mycoplasma pneumoniae-induced rash and mucositis (MIRM) is a mucocutaneous condition linked to M. pneumoniae infection.
- It affects children and young adults, often presenting with significant mucosal involvement that can resemble Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN).
- Histopathologic features of MIRM have not been extensively studied.
Purpose of the Study:
- To systematically evaluate the histopathologic changes in Mycoplasma pneumoniae-induced rash and mucositis (MIRM).
- To compare the histopathologic findings of MIRM with other mucocutaneous conditions like SJS/TEN and erythema multiforme.
- To identify distinguishing features of MIRM through histopathologic analysis.
Main Methods:
- Retrospective review of clinical and histopathologic data from eleven confirmed cases of MIRM.
- Detailed recording and analysis of clinical and histopathologic features from available biopsies.
- Comparison of histopathologic findings with clinical presentations and serological confirmation.
Main Results:
- All MIRM cases showed a vacuolar to lichenoid interface reaction with epidermal apoptotic keratinocytes.
- Subepithelial splitting and epithelial necrosis were present in approximately half of the cases, mimicking SJS/TEN.
- A subset of cases exhibited a neutrophil-rich lichenoid infiltrate, associated with leukocytosis and involvement of skin and all three mucosal sites.
Conclusions:
- Histopathologic features of MIRM are often indistinguishable from erythema multiforme or SJS/TEN.
- A neutrophil-rich lichenoid infiltrate may be a distinguishing feature in a small subset of MIRM cases.
- MIRM is considered synonymous with M. pneumoniae-associated erythema multiforme major; clinical and serologic correlation is crucial to differentiate from SJS/TEN.
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