Stevens-Johnson Syndrome and Stroke Related to Mycoplasma.

Mycoplasma pneumonia usually causes asymptomatic to mild respiratory tract infection. However, nonrespiratory manifestations are not rare with involvement of various organ including skin, cardiovascular, central nervous system. We are presenting a 43-year-old male who presented with diffuse rash, sever mucositis, confusion, and complicated by ischemic stroke; also, review of mycoplasma related stroke and Stevens-Johnson syndrome.

Introduction

Mycoplasma pneumonia is an atypical bacterium which does not have cell wall. It is one of the common respiratory pathogen usually causes asymptomatic to mild respiratory symptoms. Some people also develop extrarespiratory symptoms along with respiratory symptoms or without respiratory symptoms. Mucocutaneous diseases are common manifestation among nonrespiratory manifestation which include maculopapular or vesicular rash, urticarial, erythema multiforme (EM), and Stevens-Johnson syndrome (SJS). Other nonrespiratory manifestation includes hepatitis, pancreatitis, carditis, encephalitis, aseptic meningitis, myelitis, and glomerulonephritis.

Case Presentation

A 43-year-old previously healthy male presented to the emergency department with a 7-day history of fever, dry cough followed by the development of nonpruritic rash all over the body involving palms, soles, and mucosa associated with bleeding from his nose, mouth, palms, and soles for 2 days. On presentation, he was confused and found to have maculopapular, vesicular, and target like lesions noted over torso and extremities involving palms and soles (Figure 1-4) and severe mucositis involving lips, buccal mucosa, conjunctivae, and urethral meatus. Laboratory investigations revealed normal hemoglobin of 14.2g/dL, leukopenia with white count of 3.4 × 103/µL, thrombocytopenia of 51 × 103/µL, normal creatinine & electrolytes and mildly elevated liver enzyme with alanine aminotransferase (ALT) of 93 U/L and aspartate aminotransferase (AST) of 273 U/L. Computed tomography (CT) of lungs revealed left upper lung tree-in-bud and ground glass opacities. CT head and abdomen-pelvis were negative for an acute intracranial and intra-abdominal pathology, respectively. Cerebrospinal fluid (CSF) analysis and polymerase chain reaction (PCR) for neurotropic pathogens (Bio-Fire) were unremarkable. Skin lesions PCR for herpes simplex and varicella-zoster virus, serological test for HIV, syphilis, and hepatitis viral panel were negative. Blood, sputum, urine, and CSF cultures for bacteria and oropharynx culture for neisseria stayed sterile.

Figure 1.

Mucositis involving eyes.

Figure 2.

Maculopapular and target like lesion over chest and abdomen.

Figure 3.

Vesicular rash in hand with some ruptured and bleeding.

Figure 4.

Ischemic stroke involving right MCA.

Abbreviation: MCA, middle cerebral artery.

Respiratory viral panel of nasopharyngeal aspirate and serum IgM antibody resulted positive for M pneumoniae. Given the severity of mucosal involvement and respiratory failure, he was intubated and started on azithromycin. His leukopenia, thrombocytopenia, and liver enzymes improved slowly to normal but was still intubated due to severe desquamation of the oropharyngeal mucosa and copious secretion when left-sided weakness was noted on the ninth day of hospital stay. CT head followed by magnetic resonance imaging (MRI) of the brain revealed acute infarct with hemorrhagic transformation in the right frontal lobe involving the middle cerebral artery (MCA) territory (Figure 4). However, CT angiogram of head and neck were negative for occlusion, stenosis, aneurysm, dissection, or arteriovenous malformation in the major intracranial or neck arteries except re-demonstration of right anterior MCA territory infarct with hemorrhagic transformation. Subsequently, Echo and Doppler of limbs were done and were negative for cardiac abnormality including atrial septal defect, vegetation or deep vein thrombosis. His skin biopsy resulted findings consistent with Steven-Johnson syndrome. The patient was successfully extubated and subsequently discharged home after full recovery.

Discussion

M pneumoniae is an atypical bacterium and usually causes asymptomatic or mild respiratory tract infection. Nonrespiratory manifestations occurs in 25% of all patients with M pneumoniae infection and include encephalitis, aseptic meningitis, acute transverse myelitis, stroke, polyradiculopathy, acute disseminated encephalomyelitis (ADEM), Guillain-Barre syndrome (GBS), cranial nerve palsies, cerebellar ataxia, psychosis, hemolysis, carditis, conduction abnormalities, hepatitis, pancreatitis, glomerulonephritis, arthritis, maculopapular or vesicular rash, urticarial, EM, and SJS and mycoplasma pneumonia–associated mucositis (MPAM, also called atypical SJS).[1-7] These nonrespiratory manifestations can occur along with respiratory tract infection or independently. Extrapulmonary manifestations are common in children and young adult ranging from 6 to 21 years of age who are more prone to contract M pneumoniae respiratory infection, but uncommon in older age group.

Mucocutaneous and cutaneous diseases are more common among extrapulmonary manifestations and can occur in up to 17% patient with M pneumoniae infection. SJS is an uncommon dermal manifestation following the M pneumoniae infection and it appears to be associated more commonly than other infectious agents. SJS is characterized by an immune-mediated extensive necrosis and detachment of epidermis as this patient has had in his skin biopsy.

Central nervous system (CNS) manifestations occur in approximately 0.1% of all patients with M pneumoniae infection and up to 7% in all patients requiring hospitalization[11,12] which includes encephalitis, aseptic meningitis, acute transverse myelitis, stroke, polyradiculopathy, acute disseminated encephalomyelitis (ADEM), Guillain-Barre syndrome (GBS), cranial nerve palsies, cerebellar ataxia, and psychosis. Encephalitis and meningoencephalitis are the most common CNS complication of mycoplasma infection followed by polyradiculitis, aseptic meningitis, and cerebellar ataxia. Acute ischemic stroke (AIS) related to M pneumoniae infection is a rare manifestation, and thus far a total of 28 cases have been reported in English literature in all age group, among them only 9 were adult (Table 1)

Table 1.

Descriptions of Patients With Stroke Related to MP.

References	Age & sex	Presenting symptoms	Onset of stroke (days)	Modality of MP diag.	CSF analysis	Abnormal laboratory findings (coagulation profile and antibodies)
Dowd et al. 14	31/F	PNA	21	NA	NA	Cold agglutinin
Mulder et al. 15	30 /F	PNA	7	CF	Normal	↑fibrinogen, ↑FDP
Socan et al. 16	28/F	Cough	6	I	Normal, culture (+), PCR (+	Normal
Padovan et al. 17	36/F	URTI	8	CAA	Normal, serology (+) and PCR (+)	Positive IgM aCL,↑aPTT, positive lupus anticoagulant, ↑D-dimer
Idbaih et al. 18	35/F	PNA	21	NA	NA	NA
Siclari et al. 19	40/F	PNA	7	CAA	NA	Normal
Senda et al. 20	21/M	URTI	7	CAA	Normal	IgM (+) of aCL, ↑PT, ↑APPT, ↑fibrinogen, ↑D-dimer, ↑thrombin-antithrombin III-complex, ↓protein C
Benghanem et al 21	57/F	PNA	14	E	NA	Positive aCL and anti beta2 GP1 Ab; Hemolytic anemia
Sarathchandran et al 22	39/M	Fever and headache		NA	58 leucocytes/μL, culture (−)	NA

Abbreviations: MP, Mycoplasma pneumonia; CSF, cerebrospinal fluid; PNA, pneumonia; NA, not available; CF, complement fixation; FDP, fibrin degradation product; PCR, polymerase chain reaction; URTI, upper respiratory tract infection; CAA, cold agglutinin assay; aCL, anticardiolipin antibody; Ab, antibody.

The exact mechanism of extrapulmonary manifestations of M pneumoniae is poorly understood. These manifestations can be result of dissemination of infection resulting from direct tissue invasion by the pathogen, especially in patients with humoral immunodeficiency (eg, early onset encephalitis, myelitis, aseptic meningitis, and septic arthritis); postinfectious autoimmune phenomena (eg, late onset encephalitis, myelitis, peripheral neuropathy, cerebellar dysfunction, GBS, and SJS); vascular occlusion secondary to vasculitis or hypercoagulable state (eg, stroke); or possibly ADP ribosylating toxin.[9,23,24] Isolation of M pneumoniae in synovial fluid, pericardial fluid, and CSF has been reported,[16,25,26] which support the direct tissue invasion hypothesis; however, their numbers are limited. Moreover, only a single report has demonstrated the presence of M pneumoniae within the parenchymal brain tissue and not at all in synovial membrane and pericardium. The low reporting to isolate the organism from the infected sites could be due to difficulty in culturing the organism and lack of facility in diagnostic laboratories. The presence of autoantibodies to brain (anti-neuronal and anti-galactocerebroside antibodies) and other human tissues including well-known IgM class cold agglutinins and delayed onset of extrapulmonary manifestation like hemolysis, late onset encephalitis, GBS, ADEM after several days to a few weeks from the onset of disease support autoimmune mechanism, however, their role is not well defined. Hypercoagulability induced by M pneumoniae is another mechanism that may lead to stroke. Elevated markers of hypercoagulability (eg, fibrinogen, D-dimer), endothelial dysfunction and evolution of IgM anticardiolipin antibodies, lupus anticoagulant after M pneumoniae infection did support the hypothesis.[20,17,29] However, their numbers are limited and the presence of anticardiolipin antibodies, lupus anticoagulant were transient in contrary to antiphospholipid antibody syndrome and generally not thought to increase risk of thrombosis. The underlying mechanism of MCA occlusion in our patient remained unreveal, however, thought to be from direct CSF invasion by M pneumoniae and subsequent meningeal reaction causing vascular occlusion given presentation but arguable given normal CSF picture.

PCR-based assays are the test of choice for diagnosis of M pneumoniae infection which include direct PCR for M pneumoniae (when very high suspicion) and multiplex PCR-based assays (which detect multiple respiratory tract pathogens on a single sample). Samples used for these molecular tests in the setting of respiratory infection are nasopharyngeal swab, sputum, and bronchial alveolar lavage. Serological test with 4-fold rise in IgG titer during convalescent phase can be used as an alternative molecular test. Detection of single high IgM titer may be used as presumptive diagnosis although the specificity of the diagnostic approach is very low. Culture of the M pneumoniae is extremely difficult being a fastidious and slow-growing organism. Etiological diagnosis of extrapulmonary manifestations of the organism is difficult and made by detection of M pneumoniae by PCR or culture from the site of infection if the manifestations result from direct tissue invasion (eg, detection of mycoplasma in CSF, synovial fluid, and pericardia fluid in cases of meningitis/encephalitis, pericarditis, and septic arthritis, respectively). However, if the direct detection is unrevealing or clinical manifestations presumed to immune mediated then 4-fold rise of IgG titer during convalescent period is the primary way to make microbiological diagnosis. Sometimes presumptive diagnosis is made if extrapulmonary manifestation is concurrently present with respiratory infection and the organism is detected in respiratory tract.

Most mycoplasma infections are self-limiting; however, respiratory infection usually treated with antibiotics. Treatment with antibiotic is useful if the extrapulmonary manifestation is due to direct invasion of the organism; however, if related to autoimmune phenomenon, role of antibiotic is questionable. Macrolide, tetracycline, or fluoroquinolone classes of antibiotics are preferred, considering age of the patient and local antibiotic resistance patterns. The duration of antibiotic in pulmonary infection is usually 5 to 7 days, but in extrapulmonary infection undetermined. Use of steroid is controversial but studies have shown benefit in the setting of immune-mediated manifestations.