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Discussion: Leptospirosis is the most widespread zoonosis in the world. Human infection arises through either direct contact with infected animals or indirect contact with urine-contaminated water or soil. The prevalence of this infection is underestimated because it is typically asymptomatic and self-limited [3]. Weil’s disease is a more severe form of leptospirosis, is distinguished by the presence of jaundice, renal impairment, and hemorrhages. Pulmonary involvement occurs in 20%-70% of adult patients, and alveolar hemorrhage can occur without other typical involvement, being uncommon in pediatric age. Adolescents with severe leptospirosis may exhibit adult-like symptoms compared to children. Recognizing leptospirosis in patients with pulmonary symptoms can be difficult, especially if the patient is from a non-endemic area and lacks other characteristic signs.
This is a classic case of pulmonary hemorrhagic involvement in a patient who has no other symptom of Weil's. In this case, the authors underline the necessity of gathering information concerning epidemiological risk exposure to aid in diagnosis, as clinical suspicion and prompt treatment can achieve complete clinical recovery.
Keywords: Leptospirosis, Pediatric age, Pulmonary hemorrhagic, Zoonosis
CASE PRESENTATION
A 14-year-old male, presented to the emergency department with high fever, general malaise, cough, chest, abdominal discomfort, myalgias, and headaches for 4 days prior to admission. Later, he developed diarrhea, vomiting, diminished appetite, and difficulty walking due to severe myalgias (more severe in the calves). His prenatal, natal, postnatal, and familial histories were unremarkable, and he lived in a rural location. The initial laboratory studies showed several abnormalities, including relative neutrophilia, a mild increase in creatinine and blood urea nitrogen, leukocyturia, microscopic hematuria, elevated inflammatory markers, myoglobin of 184.8 ng/mL with remaining normal cardiac enzymes, and CRP of 217.3 mg/L. Due to abdominal and chest pain, an ultrasound scan and ECG were performed. Only homogenous hepatosplenomegaly was found. Culture studies of blood and urine did not reveal any pathogenic and all serologies were negative. The patient was admitted for monitoring, additional care, and to clarify the etiology of his condition. Throughout hospitalization, his symptoms worsened, including headaches, hemoptysis, and desaturation, prompting the introduction of supplementary oxygen. CT angiography was requested and revealed a tree-in-bud pattern, Centro acinar micronodularities, and minor ground-glass densifications throughout all lung lobes (Figures 1 & 2), which excluded pulmonary thromboembolism but raised the hypotheses of a multisystem inflammatory condition with pulmonary involvement or atypical pneumonia with systemic manifestations (including zoonotic etiologies such as Leptospirosis, Acute Q fever, Brucellosis, and Lyme disease). A complete analytical study with cerebrospinal fluid analysis and a search for atypical zoonotic etiologies were performed. Treatment with doxycycline was initiated, later combined with ceftriaxone due to pleocytosis in the cerebrospinal fluid (CSF) to cover the most likely atypical etiologies. Due to the clinical severity, with respiratory and neurological dysfunction, a single dose of immunoglobulin was administered for possible multisystem inflammatory syndrome. After 7 days of endovenous therapy, clinical improvement was observed, and subsequent evaluations showed decreasing inflammatory markers and negative CSF cultures, thus he was discharged, totally asymptomatic, on oral doxycycline (for 14 days). Following hospitalization, a urine PCR was positive for Leptospira, and because he remained clinically stable and already completed 7 days of doxycycline, antibiotherapy was discontinued.
DISCUSSION
This is a classic case of pulmonary hemorrhagic involvement in a patient who had no other symptoms of Weil's disease [2-4]. During acute illness, seronegativity has been associated with cross-reactive antibodies. To diagnose leptospirosis in such cases, molecular techniques such as real-time PCR can be used [5-8]. This is because Leptospira DNA can be detected in blood during the initial bacteremic phase of the illness, and in cerebrospinal fluid and urine a few days after the onset of symptoms [9]. Most cases of leptospirosis have a self-limited course without antimicrobial therapy [4,9]. However, some patients may experience severe complications that can lead to morbidity and mortality. For hospitalized children penicillin (250 000-400 000 units/kg/day, divided into 4-6 doses, maximum 6-12 million units/day, intravenously), doxycycline (4 mg/kg/day, divided into 2 doses, maximum 200 mg/day, intravenously), or ceftriaxone (80-100 mg/kg/day, once daily, maximum 2 g/day) can be given. The literature also mentions azithromycin, which is active against different zoonoses, however it should be considered in outpatient instances rather than moderate to severe disease. Severe illness may require supportive care such as fluid-electrolyte therapy, blood products, ventilatory support, and renal replacement therapy. In adult patients, corticosteroids may be administered when there is pulmonary involvement and vasculitis [10-12]. Our patient received supportive care and was treated with doxycycline, resulting in resolution of both clinical and laboratory findings.
- Kuitunen I, Renko M (2022) Changes in the Epidemiology of Zoonotic Infections in Children: A Nationwide Register Study in Pediatr Infect Dis J 41(4): e113-e119.
- Costa F, Hagan JE, Calcagno J, Kane M, Torgerson P, et al. (2015) Global Morbidity and Mortality of Leptospirosis: A Systematic Plos Negl Trop Dis 9(9): e0003898.
- Centers for Disease Control and Prevention (2024) Leptospirosis: Fact sheet for
- Lane AB, Dore MM (2016) Leptospirosis: A clinical review of evidence-based diagnosis, treatment and World J Clin Infect Dis 6(4): 61-66.
- Torgerson PR, Hagan JE, Costa F, Calcagno J, Kane M, et al. (2015) Global Burden of Leptospirosis: Estimated in Terms of Disability Adjusted Life Years. PLoS Negl Trop Dis 9(10): e0004122.
- Segura ER, Ganoza CA, Campos K, Ricaldi JN, Torres S, et al. (2005) Peru-United States Leptospirosis Clinical spectrum of pulmonary involvement in leptospirosis in a region of endemicity, with quantification of leptospiral burden. Clin Infect Dis 40(3): 343-351.
- Guerrier G, Hie P, Gourinat AC, Huguon E, Polfrit Y, et al. (2013) Association between age and severity to leptospirosis in children. PLoS Negl Trop Dis 7(9): e2436.
- Boertjes E, Hillebrand S, Bins JE, Oswald L (2020) Pulmonary hemorrhage in Weil's BMJ Case Rep 13(1): e227570.
- Doneray H, Keskin H, Akat H, Basaslan IH, Serifoglu Bagatir P (2023) Pediatric leptospirosis: A case report and review of literature. Eurasian J Med 55(1): S150-S156.
- American Academy of Pediatrics, Kimberlin DW, Brady MT, Jackson MA, Long SS (2018) Report of the Committee on Infectious 31st ed. Itasca, IL: American Academy of Pediatrics pp: 905.
- Kularatne SAM, Budagoda BDSS, de Alwis VKD, Wickramasinghe WMRS, Bandara JMRP, et al. (2011) High efficacy of bolus methyl prednisolone in severe leptospirosis: A descriptive study in Sri Lanka. Postgrad Med J 87(1023): 13-17.
- Azevedo AF, Miranda-Filho B, Henriques-Filho GT, Leite A, Ximenes RA (2011) Randomized controlled trial of pulse methyl prednisolone × placebo in treatment of pulmonary involvement associated with severe [ISRCTN74625030]. BMC Infect Dis 11: 186.
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