scholarly journals Increased number of pulmonary megakaryocytes in COVID-19 patients with diffuse alveolar damage: an autopsy study with clinical correlation and review of the literature

2020 ◽  
Author(s):  
Mariel F. Valdivia-Mazeyra ◽  
Clara Salas ◽  
Jesús M. Nieves-Alonso ◽  
Luz Martín-Fragueiro ◽  
Carmen Bárcena ◽  
...  
2017 ◽  
Vol 6 (2) ◽  
Author(s):  
Ana Carvoeiro ◽  
Filipa Carvalho ◽  
Nuno Montenegro ◽  
Alexandra Matias

Abstract Aim To propose a diagnostic algorithm for non-immune fetal hydrops (NIFH) of metabolic origin based on a review of the literature and on the workup of a clinical case. Background The etiology of NIFH is complex and remains unexplained in 15%–25% of patients. The appropriate work up beyond an initial approach is still not well defined but it should include screening for metabolic conditions. Inborn errors of metabolism comprise a heterogeneous group of autosomal recessive rare inherited disorders, among which lysosomal storage disorder is the most common subtype. Case description We report a case of a 30-year-old pregnant, primiparous woman, referred to a tertiary hospital at 22 weeks of gestation because of a fetal hydrops. The second trimester obstetric ultrasound showed a hydrothorax and a large subcutaneous edema. At 30 weeks of gestation, the fetal health status deteriorated and a massive hepatomegaly was detected. The metabolic study of the amniotic fluid supernatant suggested a lysosomal disease. The ominous prognosis of the condition motivated the parents to opt for a termination of pregnancy. The autopsy study confirmed the existence of a metabolic disease. Conclusion The incidence of inborn errors of metabolism may be significantly higher in NIHF than reported previously. Consequently, an extensive investigation for the etiology of NIHF including the screening for metabolic disorders seems to be crucial for a definitive diagnosis. Clinical relevance Despite the lack of treatment options for the majority of these disorders, it is of great importance to follow an established workup, in order to identify the index case as soon as possible, as pregnancy management decisions and prenatal counselling in future pregnancies will depend on a more precise diagnosis.


2015 ◽  
Vol 41 (11) ◽  
pp. 1921-1930 ◽  
Author(s):  
José A. Lorente ◽  
Pablo Cardinal-Fernández ◽  
Diego Muñoz ◽  
Fernando Frutos-Vivar ◽  
Arnaud W. Thille ◽  
...  

2005 ◽  
Vol 129 (3) ◽  
pp. 366-371 ◽  
Author(s):  
Monika Roychowdhury ◽  
Stefan E. Pambuccian ◽  
Deniz L. Aslan ◽  
Jose Jessurun ◽  
Alan G. Rose ◽  
...  

Abstract Context.—Bone marrow transplantation (BMT) is used to treat various malignant and nonmalignant disorders. Pulmonary complications are some of the most common causes of mortality in BMT recipients. Poor general health and bleeding tendency frequently preclude the use of definitive diagnostic tests, such as open lung biopsy, in these patients. Objective.—To identify pulmonary complications after BMT and their role as the cause of death (COD). Design.—The autopsy and bronchoalveolar lavage (BAL) slides and microbiology studies of BMT recipients from a 7-year period were reviewed. Results.—Pulmonary complications were identified in 40 (80%) of the 50 cases. The most common complications were diffuse alveolar damage (DAD) and diffuse alveolar hemorrhage (DAH). Pulmonary complications were the sole or 1 of multiple CODs in 37 cases (74%). All complications were more common in allogeneic BMT recipients. In 19 (51%) of the 37 cases in which pulmonary complications contributed to the death, cultures were negative. Both DAD and DAH, complications commonly reported in the early post-BMT period, were seen more than 100 days after BMT in 33% and 12% of cases, respectively. Five (83%) of 6 cases of invasive pulmonary aspergillosis diagnosed at autopsy were negative for fungi ante mortem (by BAL and cultures). Conclusions.—Pulmonary complications are a significant COD in BMT recipients, many of which, especially the fungal infections, are difficult to diagnose ante mortem. The etiology of DAD and DAH is likely to be multifactorial, and these complications are not limited to the early posttransplantation period. Autopsy examination is important in determining the COD in BMT recipients.


2013 ◽  
Vol 43 (4) ◽  
pp. 547-553 ◽  
Author(s):  
Eric A. White ◽  
Dakshesh B. Patel ◽  
Deborah M. Forrester ◽  
Christopher J. Gottsegen ◽  
Emily O’Rourke ◽  
...  

1993 ◽  
Vol 13 (5) ◽  
pp. 583-589 ◽  
Author(s):  
C. M. Coffin ◽  
K. Schechtman ◽  
F. S. Cole ◽  
L. P. Dehner

2020 ◽  
Vol 477 (3) ◽  
pp. 349-357 ◽  
Author(s):  
Hans Bösmüller ◽  
Selina Traxler ◽  
Michael Bitzer ◽  
Helene Häberle ◽  
Wolfgang Raiser ◽  
...  

Thorax ◽  
2021 ◽  
pp. thoraxjnl-2020-216714
Author(s):  
Belén Pérez-Mies ◽  
María Gómez-Rojo ◽  
Irene Carretero-Barrio ◽  
Tommaso Bardi ◽  
Amparo Benito ◽  
...  

Diffuse alveolar damage and thrombi are the most common lung histopathological lesions reported in patients with severe COVID-19. Although some studies have suggested increased pulmonary angiogenesis, the presence of vascular proliferation in COVID-19 lungs has not been well characterised. Glomeruloid-like microscopic foci and/or coalescent vascular proliferations measuring up to 2 cm were present in the lung of 14 out of 16 autopsied patients. These lesions expressed CD31, CD34 and vascular endothelial cadherin. Platelet-derived growth factor receptor-β immunohistochemistry and dual immunostaining for CD34/smooth muscle actin demonstrated the presence of pericytes. These vascular alterations may contribute to the severe and refractory hypoxaemia that is common in patients with severe COVID-19.


2020 ◽  
Vol 61 (4) ◽  
pp. 355 ◽  
Author(s):  
Francesco Del Giudice ◽  
Alex M. Kasman ◽  
Matteo Ferro ◽  
Alessandro Sciarra ◽  
Ettore De Berardinis ◽  
...  

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