# Reactive Infectious Mucocutaneous Eruption (RIME) Associated with Mycoplasma pneumoniae: Clinical and Immunological Insights from Pediatric Cases

**Authors:** David M. Matea, Raluca Isac, Estera Boeriu, Patricia Urtila, Gabriela Doros, Mihaela Bataneant, Andrada L. Oprisoni, Smaranda T. Arghirescu

PMC · DOI: 10.3390/microorganisms14020364 · 2026-02-04

## TL;DR

This paper describes three pediatric cases of RIME caused by Mycoplasma pneumoniae, highlighting its clinical features and management challenges.

## Contribution

The study provides clinical and immunological insights into RIME through case reports and literature review.

## Key findings

- RIME cases showed varied mucositis and skin involvement, including a solitary palm ulcer and widespread rash.
- Mycoplasma pneumoniae was confirmed as the etiology via IgM serology and PCR in the cases.
- Prompt recognition and multidisciplinary management are crucial for RIME due to its overlap with SJS.

## Abstract

Reactive infectious mucocutaneous eruption (RIME) is a rare pediatric condition characterized by severe mucositis, minimal cutaneous involvement, and an infectious rather than drug-induced etiology. Mycoplasma pneumoniae (M. Pneumoniae) represents the most frequently identified trigger, although an increasing number of alternative pathogens have been reported. Its clinical overlap with Stevens–Johnson syndrome (SJS) makes early recognition difficult. We reviewed literature data on the topic and described our center’s experience with three pediatric cases of M. pneumoniae-associated RIME. Medical records, laboratory results, and imaging were systematically analyzed. All patients were male, aged 2 to 12 years and originated from rural communities. Etiologic confirmation was achieved via M. pneumoniae IgM serology and/or polymerase chain reaction. Clinical exam modifications included multi-site mucositis (oral, ocular, genital) with variable skin involvement: absent in one case, a solitary palm ulcer in another, and widespread rash in the third. One patient required two hospitalizations within a six-month interval, confirming the possible relapsing phenotype of RIME. Another patient developed pneumonia, sepsis, and systemic inflammation. All received macrolide therapy, antifungals, mucosal supportive care, and systemic management as indicated. Recovery occurred within 10–21 days, with one patient exhibiting skin hyperpigmentation. These cases illustrate the heterogeneity of RIME, emphasize the importance of prompt recognition, etiology confirmation, and multidisciplinary management. RIME is a rare clinical condition in pediatric population, an uncommon but significant mucocutaneous clinical entity, important to be acknowledged by clinicians as a complication and/or extra-pulmonary manifestation of M. pneumoniae infection.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249)

## Full-text entities

- **Diseases:** mucocutaneous eruption (MESH:D003875), coagulation (MESH:D001778), bronchitis (MESH:D001991), encephalitis (MESH:D004660), congestion (MESH:D002311), infection (MESH:D007239), Chlamydia pneumoniae (MESH:D023521), COVID (MESH:D000086382), thrombocytopenia (MESH:D013921), cytotoxic (MESH:D064420), HSV (MESH:D006561), cough (MESH:D003371), vascular involvement (MESH:D057772), Oral mucositis (MESH:D013280), Ulcerative lesions (MESH:D014456), arthritis (MESH:D001168), glomerulonephritis (MESH:D005921), pericarditis (MESH:D010493), epidermal necrosis (MESH:D004814), rhinorrhea (MESH:D012818), immunodeficiency (MESH:D007153), sore throat (MESH:D010612), hematologic abnormalities (MESH:D006402), Streptococcus pneumonia (MESH:D011008), Conjunctivitis (MESH:D003231), Viral (MESH:D014777), IgG, IgA, or IgM deficiencies (MESH:D017099), necrosis (MESH:D009336), erythema (MESH:D004890), Fuch's syndrome (MESH:D005642), community-acquired pneumonia (MESH:D003147), Infectious Mucocutaneous Eruption (MESH:D003141), sepsis (MESH:D018805), oral candidiasis (MESH:D002180), bacterial (MESH:D001424), M. pneumoniae (MESH:C566367), musculoskeletal disorders (MESH:D009140), renal injury (MESH:D007674), mucosal injury (MESH:D052016), T/B cell abnormalities (MESH:D016393), hemolytic anemia (MESH:D000743), appetite loss (MESH:D001068), cardiac involvement (MESH:D006331), Guillain-Barre syndrome (MESH:D020275), cancer (MESH:D009369), EM (MESH:D004892), lymphopenia (MESH:D008231), varicella (MESH:D002644), hyponatremia (MESH:D007010), edema (MESH:D004487), meningitis (MESH:D008580), Extra (MESH:D000092225), anorexia (MESH:D000855), neurological complications (MESH:D002493), inflammation (MESH:D007249), mucocutaneous syndrome (MESH:D007897), T-cell-mediated defects (MESH:C536722), IgA deficiency (MESH:D017098), injury to (MESH:D014947), mucocutaneous disease (MESH:D004194)
- **Chemicals:** phenytoin (MESH:D010672), cephalosporin (MESH:D002511), macrolide (MESH:D018942), fluoroquinolones (MESH:D024841), valproic acid (MESH:D014635), NSAIDs (-), naproxen (MESH:D009288), tetracycline (MESH:D013752), beta-lactam (MESH:D047090), fluconazole (MESH:D015725), ampicillin (MESH:D000667), carbamazepine (MESH:D002220), sulfamethoxazole-trimethoprim (MESH:D015662), nystatin (MESH:D009761), ciprofloxacin (MESH:D002939), azithromycin (MESH:D017963), allopurinol (MESH:D000493), paracetamol (MESH:D000082), amoxicillin (MESH:D000658), acyclovir (MESH:D000212), phenobarbital (MESH:D010634), methylprednisolone (MESH:D008775), tetracyclines (MESH:D013754), piroxicam (MESH:D010894), tenoxicam (MESH:C032801), levofloxacin (MESH:D064704)
- **Species:** human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Adenoviridae (family) [taxon 10508], Haemophilus influenzae (species) [taxon 727], Homo sapiens (human, species) [taxon 9606], Norovirus (genus) [taxon 142786], Human betaherpesvirus 6 (species) [taxon 10368], Legionella pneumophila (species) [taxon 446], Treponema pallidum (species) [taxon 160], Cytomegalovirus (genus) [taxon 10358], Neisseria gonorrhoeae (species) [taxon 485], Mycoplasmoides pneumoniae (Filterable agent of primary atypical pneumonia, species) [taxon 2104], Human papillomavirus (species) [taxon 10566], Chlamydia pneumoniae (species) [taxon 83558], Streptococcus sp. 'group A' (species) [taxon 36470], Candida albicans (species) [taxon 5476], Coxsackievirus (species) [taxon 12066], Streptococcus pyogenes (species) [taxon 1314], Streptococcus pneumoniae (species) [taxon 1313], Bordetella parapertussis (species) [taxon 519], human metapneumovirus (no rank) [taxon 162145], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Bordetella pertussis (species) [taxon 520]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943772/full.md

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Source: https://tomesphere.com/paper/PMC12943772