scholarly journals Pulmonary haemorrhage in Weil’s disease

2020 ◽  
Vol 13 (1) ◽  
pp. e227570
Author(s):  
Emma Boertjes ◽  
Stefanie Hillebrand ◽  
Janneke Elisabeth Bins ◽  
Laurien Oswald

Leptospirosisis a zoonosis caused by spirochaetes from the species Leptospira. The more severe form of leptospirosis, known as Weil’s disease, is characterised by the triad of jaundice, renal impairment and haemorrhages. Pulmonary involvement occurs in 20%–70% of the patients, with severity ranging from non-productive cough to respiratory failure mainly due to pulmonary haemorrhage. Recognition of Weil’s disease in patients presenting with pulmonary symptoms can be difficult. This case illustrates a classic case of pulmonary haemorrhagic involvement in Weil’s disease.

2017 ◽  
Vol 45 ◽  
pp. 5
Author(s):  
Vinícius Bentivóglio Costa Silva ◽  
Simone Tostes de Oliveira Stedile ◽  
Renato Silva De Sousa ◽  
Marlos Gonçalves Sousa

Background: Leptospirosis is probably the most widespread and prevalent zoonosis in the world, being classified as an emerging infectious disease for humans and dogs. Sporadically, dogs may present with cough and dyspnea, indicative of pulmonary involvement, associated with interstitial pneumonia and pulmonary hemorrhage with alveolar consolidation. Such changes stem from pulmonary haemorrhagic syndrome, which has emerged as a fatal complication, being documented in some areas in Europe and little described in North America. In this sense, the present study aims to report pulmonary hemorrhagic syndrome in a dog with leptospirosis.Case: A dog with no defined breed, aged 45 days, weighing 2.2 kg, with a history of apathy, anorexia, jaundice, hematochezia and vocalisation with a two day evolution was seen. Physical examination revealed a rectal temperature of 37.2°C, icteric mucosa, capillary filling time of two seconds, respiratory rate of 80 movements per minute and heart rate of 140 beats per minute, dehydration rate estimated at 8%, prostration, adequate body score, normal cardiac sounds and clean lung fields, in addition to petechiae in the abdominal region, whose palpation evidenced the presence of fluid in intestinal loops. The blood sample sent to the macroscopic serum agglutination was reagent for the serovar Icterohaemorragiae, titration of 200. Blood count revealed leukocytosis due to neutrophilia, with left-sided deviation, eosinopenia, presence of rare hypersegmentated neutrophils, rare toxic neutrophils, mild cytoplasmic basophilia and rare reactive lymphocytes. Platelet estimation demonstrated thrombocytopenia. No haemoparasites were seen. Regarding the biochemical evaluation, there were changes in liver enzymes and markers of renal failure. Fluid therapy was used with 0.9% NaCl solution, 5 mg/ kg doxycycline intravenously every 12 h and nasogastric probe for administration of nutritional support. One day after the initial evaluation, hemoptysis and diffuse crackling occurred in pulmonary lobes on auscultation. In the radiograph of the chest, pulmonary fields were characterized by a diffuse interstitial bronchial pattern and a focal area, located in the left caudal lobe, with opacification tending to the alveolar pattern. Due to pulmonary alterations, the animal presented respiratory arrest and evolved to death. During necropsy, the macroscopic evaluation revealed a pinkish coloration pattern, with multifocal reddish areas with coalescent interspersed in the parenchyma and hypocrepitation. Regarding the morphology, multifocal hemorrhagic pneumonia was observed, focally extensive, moderate to severe.Discussion: Recently, pulmonary haemorrhagic syndrome has emerged as a severe form of leptospirosis in many species, including humans and dogs. Patients may develop fulminant pulmonary haemorrhage and result in a high mortality rate. Physiopathogenesis is poorly understood, however, it is believed that there is a multifactorial pathogenesis involving factors related to both pathogen and host, such as immunological mechanisms and coagulopathies. Studies in humans have shown a better evolution after the use of cyclophosphamide, but the benefits of this therapy have not yet been determined in dogs. Therefore, pulmonary haemorrhagic syndrome should be considered in patients with leptospirosis who show respiratory changes, due to the severity of the clinical signs and the high lethality associated with this clinical condition.


1995 ◽  
Vol 47 (5) ◽  
pp. 224-229 ◽  
Author(s):  
J DEKONING ◽  
J VANDERHOEVEN ◽  
A MEINDERS

2021 ◽  
Vol 1 (1) ◽  
pp. 023-026
Author(s):  
Sanjay Sud

This study present the details of a case of classical Weil’s Disease, which is a severe form of leptospirosis, presenting with symptoms of fever, jaundice, joint pain, haemorrhagic manifestations and renal failure. Leptospirosis is an uncommon but not rare health problem in a tropical country like India. Clinical manifestations along with the laboratory findings are elaborated, so that a differential diagnosis from other common ailments with similar manifestations can be considered in favour of the disease. An early empirical management on high clinical suspicion can help to avoid multi-organ dysfunction and mortality associated with this disease.


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Alexander Winkler ◽  
Emanuel Zitt ◽  
Hannelore Sprenger-Mähr ◽  
Afschin Soleiman ◽  
Manfred Cejna ◽  
...  

Abstract Background Anti-glomerular basement membrane disease (GBM) disease is a rare autoimmune disease causing rapidly progressive glomerulonephritis and pulmonary haemorrhage. Recently, an association between COVID-19 and anti-glomerular basement membrane (anti-GBM) disease has been proposed. We report on a patient with recurrence of anti-GBM disease after SARS-CoV-2 infection. Case presentation The 31-year-old woman had a past medical history of anti-GBM disease, first diagnosed 11 years ago, and a first relapse 5 years ago. She was admitted with severe dyspnoea, haemoptysis, pulmonary infiltrates and acute on chronic kidney injury. A SARS-CoV-2 PCR was positive with a high cycle threshold. Anti-GBM autoantibodies were undetectable. A kidney biopsy revealed necrotising crescentic glomerulonephritis with linear deposits of IgG, IgM and C3 along the glomerular basement membrane, confirming a recurrence of anti-GBM disease. She was treated with steroids, plasma exchange and two doses of rituximab. Pulmonary disease resolved, but the patient remained dialysis-dependent. We propose that pulmonary involvement of COVID-19 caused exposure of alveolar basement membranes leading to the production of high avidity autoantibodies by long-lived plasma cells, resulting in severe pulmonary renal syndrome. Conclusion Our case supports the assumption of a possible association between COVID-19 and anti-GBM disease.


1937 ◽  
Vol 12 (3) ◽  
pp. 123-125
Author(s):  
G. Bewley ◽  
J. G. Wilson

BMJ ◽  
1946 ◽  
Vol 2 (4482) ◽  
pp. 813-814 ◽  
Author(s):  
H. Jackson ◽  
S. Oleesky

BMJ ◽  
1952 ◽  
Vol 2 (4781) ◽  
pp. 427-428
Author(s):  
A. A. Morgan

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