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Revista de la Facultad de Medicina Humana
versión impresa ISSN 1814-5469versión On-line ISSN 2308-0531
Rev. Fac. Med. Hum. vol.24 no.4 Lima oct./dic. 2024 Epub 31-Oct-2024
http://dx.doi.org/10.25176/rfmh.v24i4.6519
Case Report
Dengue infection in a patient with systemic lupus erythematosus: a case report
1. General Physician specializing in Internal Medicine. Unidad Médica de Alta Especialidad Hospital de Especialidades, Centro Médico Nacional Gral. de Div. Manuel Ávila Camacho, Instituto Mexicano del Seguro Social, Puebla de Zaragoza, Puebla, Mexico.
Systemic Lupus Erythematosus (SLE) is an autoimmune disease caused by an autoreactive B and T cell response with loss of immune tolerance to self-antigens. It manifests with asthenia, fever, myalgias, arthralgias, skin rash and fatal organ damage. Dengue is a zoonotic disease caused by the dengue virus (DENV), transmitted by mosquitoes of the Aedes aegypti species. Diagnostic suspicion is made in the presence of acute febrile syndrome with clinical manifestations and demographic history. Confirmation is made through virus detection by RT-PCR, or the structural NS1 protein. The present case report is a 58-year-old woman with data of lupus exacerbation and with clinical manifestations suggestive of Dengue fever, with a history of travel to an endemic area. The confirmatory RT-PCR test leads to appropriate medical treatment. The importance of the case lies in differentiating the diagnosis in a timely manner.
Keywords: Systemic lupus erythematosus; cutaneous lupus erythematosus; dengue; viral zoonoses; fever.
INTRODUCTION
Systemic lupus erythematosus (SLE) is a chronic, inflammatory, autoimmune disease characterized by an autoreactive response of B and T cells, leading to a loss of immune tolerance to self-antigens. Its clinical manifestations can be mild, moderate, or, in more severe cases, life-threatening. It is characterized by symptoms such as asthenia, fever, myalgia, arthralgia, skin rash, and potentially fatal organ damage both at the onset and during disease activity (1).
Dengue is a zoonosis transmitted by Aedes aegypti mosquitoes and causes fever, headache, myalgia, arthralgia, and transient skin rashes. In severe cases, it can lead to respiratory difficulties, hemorrhage, and multiple organ failure (2).
The objective of this case report is to describe the clinical presentation of dengue in a patient with SLE.
CASE REPORT
A 58-year-old woman, originally from the state of Chiapas, and a resident of the state of Puebla for the last 10 years, was diagnosed with lupus involving mucocutaneous and joint manifestations since 2019. At the time of this report, the patient was undergoing treatment with chloroquine 150 mg, azathioprine 90 mg, and prednisone 7.5 mg every 24 hours. She had also been diagnosed with systemic arterial hypertension since 2019, for which she was being treated with valsartan, amlodipine, and hydrochlorothiazide (5 mg/160 mg/12.5 mg) every 24 hours.
On January 9, 2023, she presented with a fever of 38.9°C, holocranial headache, hyporexia, asthenia, and arthralgia. She self-medicated with 500 mg of acetaminophen, resulting in partial improvement. Two days later, her fever returned (38.9°C), accompanied by nausea and one episode of gastrointestinal vomiting. She was hospitalized for febrile syndrome under study, and her maintenance treatment for SLE was suspended.
Upon admission, she had a fever of 38.9°C and knee pain. Physical examination revealed erythematous papules on the eyelids and malar region, with no ulcers in the nasal or oral mucosa. A maculopapular rash with erythematous papules and mild confluent scaling was noted on the anterior chest and the right posterior hemithorax. No cardiopulmonary or abdominal involvement was observed. The upper limbs showed a maculopapular rash, and the lower limbs exhibited limited flexion and extension due to knee pain. The results of blood count, blood chemistry, and coagulation tests are shown in Table 1. The general urinalysis reported: cloudy brown appearance, 100 leukocytes/µL, negative nitrites, 150 mg/dL proteins, 250 erythrocytes/µL, 30-41 leukocytes per field, 40-50 erythrocytes per field, 2+ bacteria, 1+ epithelial cells, 0-1 hyaline casts, and 0-1 granular casts. A rapid antigen test for SARS-CoV-2 was negative.
The patient received treatment with acetaminophen 1 g every 8 hours and Hartmann solution 1000 ml IV every 24 hours. She had a slow evolution with persistent fever and increased arthralgia and edema in her lower limbs. Upon further questioning, the patient reported a recent trip to an endemic area (state of Chiapas) one week before the onset of symptoms. The Rumpel-Leede test was performed and reported positive. Epidemiology was notified of a probable dengue diagnosis with warning signs (thrombocytopenia). A real-time polymerase chain reaction (RT-PCR) test for dengue was performed. Treatment with chloroquine 150 mg every 24 hours and acetaminophen was resumed; azathioprine was not restarted. The patient showed improvement, without hemorrhage despite severe thrombocytopenia. The RT-PCR result, three days after the sample was taken, was positive for dengue (DENV-3 serotype). With the resolution of symptoms and no warning signs, she was discharged home after five days of hospitalization.
DISCUSSION
Systemic lupus erythematosus (SLE) has a global incidence of 6.73 per 100,000 individuals in Caucasian populations and 31.4 per 100,000 in African American populations annually (3). The clinical findings of SLE are shown in Table 2 (4). The criteria of the European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) allow for the classification of the clinical presentation of SLE by systems and organs (Table 3) (5). The SLEDAI (Systemic Lupus Erythematosus Disease Activity Index), later modified as MEX-SLEDAI for the Mexican population, evaluates disease activity during lupus exacerbation (15), though the patient did not meet the criteria for exacerbation.
Initial treatment for SLE includes antimalarials, while glucocorticoids are recommended for controlling acute attacks and maintenance therapy (6).
Dengue is a zoonotic disease caused by the dengue virus (DENV), transmitted by Aedes aegypti mosquitoes (8). In Mexico, 12,671 cases were reported in 2022 (with an incidence of 9.74 per 100,000 inhabitants); 57% of these cases were concentrated in the states of Sonora, Veracruz, Estado de México, Tabasco, and Chiapas, with serotypes DENV-2 (56.03%) and DENV-3 (24.93%) being the most prevalent (7).
According to the World Health Organization (WHO), dengue is classified as: 1) Dengue without warning signs (suspected dengue due to residence in or travel to endemic areas, fever, and at least two symptoms such as nausea, vomiting, myalgia, arthralgia, leukopenia, or a positive tourniquet test); 2) Dengue with warning signs (same as the previous definition, plus any warning symptom such as abdominal pain, serositis, hemorrhages, altered mental status, visceromegaly, or a sudden drop in platelet count); and 3) Severe dengue (includes the previous signs plus evidence of organ or system damage, including multiple organ failure) (7). In this case, the patient fell under the category of dengue with warning signs due to the presence of thrombocytopenia.
The diagnostic suspicion is based on acute febrile syndrome with clinical manifestations and demographic history. The Rumpel-Leede or tourniquet test is recommended by the WHO due to its ease of application and utility in decision-making. The test involves inflating the sphygmomanometer cuff on the upper arm to a point midway between the individual’s systolic and diastolic pressures and maintaining it inflated for five minutes. After deflation and two minutes of rest, the number of petechiae below the antecubital fossa is counted. The test is considered positive if more than 10 petechiae are present within a square inch of skin on the arm (16). Although the test has documented low sensitivity and specificity (58%, 95% CI: 43%-71%; and 71%, 95% CI: 60%-80%, respectively), it remains recommended as a decision-support tool in resource-limited areas (16).
Confirmation of dengue is achieved through the detection of the virus via RT-PCR or the identification of the NS1 structural protein or specific IgM (11). Treatment is symptomatic, and depending on the severity, most cases are managed on an outpatient basis. Patients with comorbidities or signs of severe disease should be hospitalized (8).
In the clinical case presented, the patient, who had an exacerbation of lupus, revealed a recent trip to an endemic dengue area during the medical history interview. Diagnostic suspicion was based on the positive Rumpel-Leede test, which supported the decision to perform the confirmatory RT-PCR test, alongside laboratory results and patient history.
The use of immunosuppressants such as azathioprine and prednisone may have facilitated the severity of dengue in this case, as both drugs are known to cause bone marrow toxicity.
The variations in thrombocytopenia further supported the classification of the patient’s case as dengue with warning signs, which led to the management with intravenous fluids, up to 1000 milliliters in addition to oral intake. The patient experienced third-space fluid leakage, primarily in the lower limbs, during the first 48 hours of hospitalization, which resolved by the time of discharge.
Table 1 Laboratory results obtained during the hospital stay
Parameter | 03/12/2024 | 03/13/2024 | 03/14/2024 | |
COMPLETE BLOOD COUNT (CBC) | Hemoglobin (g/dL) | 14.6 | 15.62 | 14.86 |
Hematocrit | 44.3 | 47.99 | 45.26 | |
Platelets | 79,800 | 53,000 | 34,000 | |
Citrated platelets | ||||
Leukocytes (cel/uL) | 4,100 | 3,290 | 5,060 | |
BLOOD CHEMISTRY | Glucose (mg/dL) | 101 | ||
Creatinine (mg/dL) | 0.71 | |||
Na+ (mmol/L) | 135 | |||
K+ (mmol/L) | 4.4 | |||
Cl- (mmol/L) | 103 | |||
AST (mg/dL) | 82 | |||
ALT (mg/dL) | 19 | |||
Total Bilirubin (mg/dL) | 0.31 | |||
Direct Bilirubin (mg/dL) | 18 | |||
Indirect Bilirubin (mg/dL) | 0.13 | |||
Albumin (mg/dL) | ||||
LDH (UI/L) | 601 | |||
COAGULATION TIMES | Prothrombin Time (PT) (seconds) | 12.5 | ||
Control Prothrombin Time (seconds) | 11.5 | |||
Partial Thromboplastin Time (PTT) (seconds) | 35.6 | |||
International Normalized Ratio (INR) | 1.09 |
Table 2 Spectrum of clinical symptoms in Systemic Lupus Erythematosus (measurement of lupus activity and cumulative damage in patients with Systemic Lupus Erythematosus) (4)
Affected system | Symptom | % of occurrence | |
At presentation | During lupus activation | ||
General | Fatigue | 50 | 74 to 100 |
Fever | 36 | 40 to 80 | |
Weight changes | 21 | 44 to 60 | |
Myalgia and Arthralgia | 62 to 67 | 83 to 95 | |
Tegumentary | General | 73 | 80 to 91 |
Malar rash | 73 | 80 to 91 | |
Photosentivity | 29 | 41 to 60 | |
Mucosal Membrane Lesions | 10 to 21 | 27 to 52 | |
Alopecia | 32 | 18 to 71 | |
Raynaud's Phenomenon | 17 to 33 | 22 to 71 | |
Purpura | 10 | 15 to 34 | |
Urticaria | 1 | 4 to 8 | |
Renal | General | 16 to 38 | 34 to 73 |
Nephrosis | 5 | 11 to 18 | |
Gastrointestinal | Esophagitis, Pseudo-obstruction | 18 | 38 to 44 |
Splenomegaly | 5 | 9 to 20 | |
Hepatomegaly | 2 | 7 to 25 | |
Pulmonary | General | 2 to 12 | 24 to 98 |
Pleuritis | 17 | 30 to 45 | |
Effusion | 24 | ||
Pneumonia | 29 | ||
Cardiovascular | General | 15 | 20 to 46 |
Pericarditis | 8 | 8 to 48 | |
Murmurs | 23 | ||
ECG Changes | 34 to 70 | ||
Lymphadenopathy | 7 to 16 | 21 to 50 | |
Central Nervous System | General | 12 to 21 | 25 to 75 |
Functional | Majority | ||
Psychosis | 1 | 5 to 52 | |
Seizures | 0.5 | 2 to 20 |
Table 3 Classification criteria of the European Alliance of Associations for Rheumatology (EULAR)/American College of Rheumatology (ACR) for Systemic Lupus Erythematosus (SLE) 2019
Entry Criterion (Required for classifying SLE) | ||
ANA (antinuclear antibodies) at a titer >1:80 on Hep-2 cells or an equivalent positive test (at any time). | ||
Domains and Clinical Criteria | Score | |
Constitutional | ||
Fever (>38 °C) | 2 | |
Hematologic | ||
Leukopenia (<4,000 cells/L) | 3 | |
Thrombocytopenia (<100,000 cells/L) | 4 | |
Autoimmune hemolysis (confirmed) | 4 | |
Neuropsychiatric | ||
Delirium (characterized by changes in consciousness or reduced ability to concentrate; development of symptoms <2 days; symptom fluctuation throughout the day; acute/subacute changes in cognition or behavior) | 2 | |
Psychosis (characterized by hallucinations and in the absence of delirium) | 3 | |
Seizures (generalized or focal) | 5 | |
Mucocutaneous | ||
Non-scarring alopecia (confirmed by a physician) | 2 | |
Oral ulcers (confirmed by a physician) | 2 | |
Subacute cutaneous lupus or discoid lupus (confirmed by a physician. If a skin biopsy is performed, typical changes must be present) | 4 | |
Acute cutaneous lupus (confirmed by a physician. If a skin biopsy is performed, typical changes must be present) | 6 | |
Serosal | ||
Pleural or pericardial effusion (evidenced by imaging) | 5 | |
Acute pericarditis (2 or more than 1) Pericardial chest pain, 2) Pericardial rub, 3) ECG showing new generalized ST elevation or PR depression, 4) New or worsening pericardial effusion confirmed by imaging) | 6 | |
Musculoskeletal | ||
Joint involvement (either: 1) Synovitis involving two or more joints; or 2) Tenderness in two or more joints with at least 30 minutes of morning stiffness) | 6 | |
Renal | ||
Proteinuria (>0.5 g in 24 hours) | 4 | |
Renal biopsy reporting lupus nephritis class II or V | 8 | |
Renal biopsy reporting lupus nephritis class III or IV | 8 | |
Domains and immunology criteria | Score | |
Antiphospholipid antibodies | ||
Anticardiolipin antibodies [IgA, IgG, or IgM at medium or high titer (>40 phospholipid units A (APL), GPL, or MPL, or >99th percentile)] or | 2 | |
Positive anti-B2GP1 antibodies (IgA, IgG, or IgM) or | ||
Positive lupus anticoagulant | ||
Complement Proteins | ||
Low C3 or low C4 | 3 | |
Low C3 and low C4 | 4 | |
SLE-Specific Antibodies | ||
Anti-dsDNA antibodies or | 6 | |
Anti-Smith antibodies |
Classification of SLE requires: 1) an entry criterion + 2) a total score of ≥10 points, and 3) at least one clinical criterion. A criterion should not be counted if there is a more likely explanation than SLE. The occurrence of a criterion on one or more occasions is sufficient, and the criteria do not need to occur simultaneously. Within each domain, only the highest-weighted criterion is counted toward the total score if more than one is present (Clinical manifestations and diagnosis of systemic lupus erythematosus in adults) (5).
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8Article published by the Journal of the faculty of Human Medicine of the Ricardo Palma University. It is an open access article, dis-tributed under the terms of the Creatvie Commons license: Creative Commons At-tribution 4.0 International, CC BY 4.0 (https://creativecommons.org/licenses/by/4.0/), that allows non-commercial use, distribution and reproduction in any medium, provided that the original work is duly cited. For commercial use, please contact revista.medicina@urp.edu.pe.
Received: May 17, 2024; Accepted: August 20, 2024