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1.
Infez Med ; 28(4): 507-515, 2020 Dec 01.
Article in English | MEDLINE | ID: mdl-33257624

ABSTRACT

The gastrointestinal system may be affected by COVID-19 infection with an incidence variable from 3% up to 79%. Several works show that the pancreas, both in its exocrine and endocrine function, can be affected by this viral infection, although this organ has been poorly analyzed in this current epidemic context. This mini-review aims to provide a summary of available studies on exocrine pancreas involvement during COVID-19 infection. A search through MEDLINE/PubMed was conducted on the topic in hand. With regard to exocrine function, some studies highlight the presence of an associated hyperenzymemia (hyperamylasemia, hyperlipasemia), while others describe isolated and rare cases of acute pancreatitis. More attention should be paid to pancreatic impairment in subjects with COVID-19, as this may prove to be one of the elements aggravating its clinical course. Indeed, acute pancreatitis, especially when presenting in severe forms with hyperstimulation of the pro-inflammatory response, may represent a crucial factor in the progression of COVID-19, entailing both an increase in hospitalization days and in mortality rate.


Subject(s)
COVID-19/enzymology , Pancreas, Exocrine/enzymology , Pancreatitis/enzymology , SARS-CoV-2 , COVID-19/complications , Disease Progression , Humans , Hyperamylasemia/virology , Lipase/blood , Pancreatitis/virology
3.
Dig Dis Sci ; 60(9): 2590-603, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25972150

ABSTRACT

AIM: Although Ebola virus infection (EVI) clinically presents with common, prominent, gastroenterologic manifestations, this subject has not been previously reviewed. This work critically and comprehensively reviews this subject. METHODS: This study is a comprehensive literature review generated by computerized search of literature, supplemented by review of monographs and textbooks in pathology, gastroenterology, infectious diseases, and virology. RESULTS: Common gastrointestinal manifestations include diarrhea-70 %, nausea and vomiting-60 %, and abdominal pain-45 %. The diarrhea and nausea and vomiting frequently produce profound, life-threatening hypovolemia requiring intravenous administration of crystalloid solutions, and frequently produce electrolyte disorders requiring electrolyte supplementation. Although gastrointestinal hemorrhage was commonly reported in early epidemics, its frequency has decreased to 10 % with prevention of disseminated intravascular coagulation. Hyperamylasemia is commonly reported, but the frequency of pancreatitis is unknown. The mean serum AST and ALT levels are each about 200/UL, with an unusual pattern for viral hepatitis of AST > ALT. The serum alkaline phosphatase averages about 160 IU/L, whereas the total bilirubin averages about 0.8 mg/dL. Risks of contracting infection during endoscopy performed on infected patients are unknown, but may be significant, as indicated by hundreds of healthcare workers contracting EVI during epidemics before instituting strict infectious control measures and anecdotal evidence of one endoscopist contracting EVI from performing endoscopy on an infected patient. CONCLUSIONS: Physicians must be vigilant for gastroenterologic manifestations of EVI for appropriate diagnosis and therapy. This work should stimulate clinicopathologic studies to improve the current understanding of the gastroenterologic pathophysiology. Endoscopy is currently not standardly recommended to evaluate diarrhea, nausea and vomiting, or abdominal pain associated with EVI due to potential risks, but may be considered for endoscopic therapy for active, life-threatening, GI hemorrhage.


Subject(s)
Gastrointestinal Hemorrhage/virology , Hemorrhagic Fever, Ebola/complications , Hemorrhagic Fever, Ebola/therapy , Abdominal Pain/virology , Alanine Transaminase/blood , Aspartate Aminotransferases/blood , Diarrhea/virology , Endoscopy, Gastrointestinal/methods , Hemorrhagic Fever, Ebola/diagnosis , Hemorrhagic Fever, Ebola/epidemiology , Hemorrhagic Fever, Ebola/transmission , Humans , Hyperamylasemia/virology , Nausea/virology , Vomiting/virology
4.
Int J Hematol ; 84(5): 438-40, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17189226

ABSTRACT

Cytomegalovirus (CMV)-associated pancreatitis is rare after allogeneic hematopoietic stem cell transplantation (SCT). We describe a patient who developed pancreatic hyperamylasemia and hyperlipasemia in association with CMV infection after cord blood transplantation (CBT). A 31-year-old man with acute myelogenous leukemia underwent CBT. A neutrophil count consistently greater than 500/microL was achieved on day +21. Positive results for CMV antigenemia on days +35 and +67 prompted 2 courses of preemptive therapy with ganciclovir or foscarnet. The CMV antigenemia value again became positive on day +134. On day +141, serum amylase and lipase activities markedly increased to 1221 IU/L and 894 IU/L, respectively. The patient had no abdominal symptoms. Ultrasonography and computed tomography results showed no abnormalities of the pancreas. A diagnosis of possible pancreatitis was made. After the initiation of foscarnet therapy, the CMV antigenemia results soon became negative, and serum amylase and lipase activities returned to normal. Therefore, CMV infection was considered to play a major role in the development of pancreatic hyperamylasemia and hyperlipasemia in our patient. The present report indicates that CMV infection should be included in the differential diagnosis for patients with pancreatic hyperamylasemia after SCT.


Subject(s)
Cord Blood Stem Cell Transplantation , Cytomegalovirus Infections/etiology , Hyperamylasemia/etiology , Leukemia, Myeloid, Acute/complications , Pancreatitis/etiology , Adult , Amylases/blood , Antiviral Agents/administration & dosage , Cytomegalovirus Infections/blood , Cytomegalovirus Infections/diagnosis , Cytomegalovirus Infections/drug therapy , Foscarnet/administration & dosage , Ganciclovir/administration & dosage , Humans , Hyperamylasemia/blood , Hyperamylasemia/diagnosis , Hyperamylasemia/drug therapy , Hyperamylasemia/virology , Leukemia, Myeloid, Acute/blood , Leukemia, Myeloid, Acute/therapy , Male , Pancreatitis/blood , Pancreatitis/diagnosis , Pancreatitis/drug therapy , Pancreatitis/virology , Transplantation, Homologous
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