Asymptomatic syphilitic massive necrosis of the spleen in late syphilis

2013 ◽  
Vol 24 (11) ◽  
pp. 912-915
Author(s):  
Nemanja Radojevic ◽  
Filip Vukmirovic ◽  
Ivana Curovic ◽  
Miodrag Soc
2021 ◽  
pp. 104063872110258
Author(s):  
Eve M. Manthorpe ◽  
Ian V. Jerrett ◽  
Grant T. Rawlin ◽  
Lucy Woolford

Acute bovine liver disease (ABLD) is a sporadic hepatic disease affecting cattle in southern Australia, characterized histologically by striking periportal hepatocellular necrosis. The cause of ABLD is unknown; however, the seasonality and acute presentation of outbreaks suggest mycotoxin involvement. We describe here the clinical and pathologic findings of ABLD in 45 naturally affected cattle from 13 outbreaks occurring from 2010 to 2019 in Victoria, Australia. Outbreaks occurred in herds located along the southern coastal plain of Victoria and were observed most frequently in lactating dairy cattle. Clinical signs commonly included a combination of mild photosensitization, progressive neurologic signs, and hypogalactia, which preceded death by ≤ 48 h. All affected animals had marked elevations in activities of glutamate dehydrogenase, aspartate aminotransferase, and gamma-glutamyl transferase. At autopsy, the most common lesions were serosal petechiae and/or gastrointestinal hemorrhage, and hepatomegaly with a pronounced hepatic reticular pattern. The principal histologic lesion was widespread—severe periportal hepatocellular coagulative necrosis and erythrocyte pooling—which often extended to massive necrosis. Lesions in other organs were uncommon. Our study of ABLD suggests involvement of a potent hepatotoxin that is either directly cytopathic or requires bioactivation by periportal-specific enzymes.


1970 ◽  
Vol 46 (2) ◽  
pp. 132-134
Author(s):  
J Towpik ◽  
E Nowakowska

2001 ◽  
Vol 40 (2) ◽  
pp. 127-130 ◽  
Author(s):  
Kosuke KASHIWABARA ◽  
Masakazu TOYONAGA ◽  
Yuji YAMAGUCHI ◽  
Hiroyuki NAKAMURA ◽  
Seigo HIRAYAMA ◽  
...  

1949 ◽  
Vol 89 (1) ◽  
pp. 69-92 ◽  
Author(s):  
Robert Rustigian ◽  
Alwin M. Pappenheimer

A study has been made of the local effects following intramuscular injection of various neurotropic viruses. Early massive necrosis of muscle fibers accompanied by edema and acute inflammatory reaction is produced by Jungeblut's SK virus even in low concentrations. Similar but more slowly developing lesions follow the introduction of mouse encephalomyelitis GD-VII and FA strains. Strain 4727 (TO type) produces inflammatory changes with fibrosis in the intermuscular septa and necrosis of scattered individual fibers. The relatively avirulent FV strain (TO type) was not pathogenic for skeletal muscle. The Mitchell strain of lymphocytic choriomeningitis virus gives rise to a profuse lymphocytic and monocytic infiltration of the fat and connective tissue but does not cause necrosis of muscle fibers. No significant lesions resulted from intramuscular injection of the murine-adapted human poliomyelitis Lansing virus, the HF strain of herpes, a strain of Eastern equine encephalitis virus, or a still unidentified demyelinating mouse virus. Evidence is presented that the mouse encephalomyelitis virus GD-VII and Jungeblut's SK virus multiply locally in the injected limb. The GD-VII virus has been passed through four muscle to muscle passages and muscle lesions have been elicited at the same time. Specific and complete protection against myositis was obtained by anti-GD-VII and anti-SK rabbit sera.


1930 ◽  
Vol 26 (9) ◽  
pp. 943-943
Author(s):  
A. Dmitriev

Abstracts. Venereology and Dermatology. Scrofuloderma "bridges" as a rare form of late syphilis .. Schmidt. (Derm. Ztsch. Bd. 57, H. 5) describes a case clinically similar to scrofuloderma, where the picture showed the presence of typical "bridges" - scars. so common in scrophuloderma. However, the study of these scars by sections gave a typical picture for a syphilitic process. The specific treatment of this case was soon brilliant.


2020 ◽  
Vol 7 (1) ◽  
pp. 11-16
Author(s):  
Héctor O. Rodríguez ◽  

Background Sudden death is the principal cause of fatality in Chagas disease, afflicting to non-symptomatic patients younger than 50-years. For this, sudden death associated with chagasic malignant arrhythmias is underdiagnosed and their pathophysiological basis is poorly understood. Aims In this sense, this work aimed to analyze the histopathological alterations in cardiac structures specialized in the generation/conduction of action potential in an anatomopathological case of non-diagnosed sudden death living in a Chagasic endemic area. Methods The donor was a woman, 62-year-old, which ingressed without vital signs to the emergency room of “Antonio María Pineda” hospital, without any apparent antecedents of cardiac disease. The gross examination was normal, with no external evidence of structural/ischemic disease. Results Microscopic examination revealed nodal like cell depopulation, microvascular disturbances, chronic myocarditis with mononuclear and mast cell infiltrate plus extracellular matrix reaction, and profuse damage of neural structures placed in nodal region. Amastigote nest of Trypanosoma cruzi (T. cruzi) was detected. Conclusion These findings suggest a complex association among parasite persistence, sinus disease, micro-ischemia foci, and neural inflammation in the genesis of malignant arrhythmias of Chagas disease despite the absence of structural disease or massive necrosis. It is important to perform a protocol of examination for no explained sudden death cases in chagasic endemic countries, to avoid misdiagnosed of sudden death associated with Chagas disease.


1930 ◽  
Vol 26 (3) ◽  
pp. 330-330
Author(s):  
A. Dmitriev

Abstracts. Syphilis. Treatment of early and late syphilis with malaria. Jacobs and Vonwinkel (Derm. Ztsch. Bd. 57. H. 5) in most cases carried out a mixed course consisting of 12-15 injections of Ві and, like "Nachkur", in order to influence malaria, 4-5 gr. salvarsan'a. The intervals between vaccinations are on average 6 months. Along with the treatment, a blood test (RW, SJ, and MTR) was performed, as well as cerebrospinal fluid (Non ne, Weichbrodt or Pandy, pleocytosis and reaction with Goldsol).


2020 ◽  
Vol 9 (5) ◽  
pp. 1420 ◽  
Author(s):  
Michał Kukla ◽  
Karolina Skonieczna-Żydecka ◽  
Katarzyna Kotfis ◽  
Dominika Maciejewska ◽  
Igor Łoniewski ◽  
...  

The novel coronavirus SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) infection has been predominantly linked to respiratory distress syndrome, but gastrointestinal symptoms and hepatic injury have also been reported. The mechanism of liver injury is poorly understood and may result as a consequence of viral hepatitis, systemic inflammatory response, gut barrier and microbiome alterations, intensive care treatment or drug toxicity. The incidence of hepatopathy among patients with coronavirus disease 2019 (COVID-19) is unclear, but studies have reported liver injury in patients with SARS and Middle East respiratory syndrome (MERS). We aimed to systematically review data on the prevalence of hepatic impairments and their clinical course in SARS and MERS Coronaviridae infections. A systematic literature search (PubMed/Embase/Cinahl/Web of Science) according to preferred reporting items for systematic review and meta-analysis protocols (PRISMA) was conducted from database inception until 17/03/2020 for studies that evaluated the incidence of hepatic abnormalities in SARS CoV-1, SARS CoV-2 and MERS infected patients with reported liver-related parameters. A total of forty-three studies were included. Liver anomalies were predominantly mild to moderately elevated transaminases, hypoalbuminemia and prolongation of prothrombin time. Histopathology varied between non-specific inflammation, mild steatosis, congestion and massive necrosis. More studies to elucidate the mechanism and importance of liver injury on the clinical course and prognosis in patients with novel SARS-CoV-2 infection are warranted.


2019 ◽  
Vol 2019 (7) ◽  
Author(s):  
Takashi Sakai ◽  
Tomohiro Miyoshi ◽  
Shigeki Umemura ◽  
Jun Suzuki ◽  
Shoko Nakasone ◽  
...  

Abstract Pulmonary sclerosing pneumocytoma (PSP) is pathologically classified as an adenoma and behaves in a benign manner. However, some cases of PSP displayed pathologically malignant behavior, such as lymph node metastasis and necrosis. A 64-year-old woman was referred to our hospital complaining of a cough and breathlessness. Histopathological analysis of the resected specimen by left pneumonectomy and lymph node dissection revealed a large PSP measuring 15 × 14 cm in size, with massive necrosis and vascular invasion. This case was the largest ever reported and suggested that clinico-histological presentation of PSP sometimes showed an aggressive phenotype like advanced lung cancer.


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