Severe Acute Pancreatitis in Autopsies Associated With Surgeries and Severe Inflammatory Diseases.


Journal

Pancreas
ISSN: 1536-4828
Titre abrégé: Pancreas
Pays: United States
ID NLM: 8608542

Informations de publication

Date de publication:
Historique:
entrez: 6 11 2019
pubmed: 7 11 2019
medline: 22 9 2020
Statut: ppublish

Résumé

We clarified clinicopathological characteristics of acute pancreatitis in terminal patients. Pathological changes in the entire pancreas from serial autopsies (N = 183) classified lesions into the following 3 categories: focal neutrophil infiltration, focal necrotizing pancreatitis, and diffuse necrotizing pancreatitis. The former two are possible precursors of diffuse necrotizing pancreatitis. Immunohistochemical staining was performed to analyze pancreatic stellate cells and inflammatory cells. There were pathologically acute pancreatitis in 45 patients (24.6%), and no patients were diagnosed with it before autopsy. Focal neutrophil infiltration was present in 22 cases, focal necrotizing pancreatitis in 18 cases, and diffuse necrotizing pancreatitis in 5 cases. Severe inflammatory disease and surgery were associated with acute pancreatitis. Sepsis due to viral or bacterial infection was the most common cause of acute pancreatitis. Patients with diffuse necrotizing pancreatitis showed low white blood cell counts, while amylase levels were not increased. Increase in α-smooth muscle actin and nestin-positive stellate cell numbers in acute pancreatitis was correlated to increase in numbers of CD34-positive vascular endothelium, CD68- or CD163-positive macrophages, CD138-positive plasmacytes, CD3-positive T lymphocytes, and myeloperoxidase-positive leucocytes. Necrotizing pancreatitis without typical clinical signs was frequently detected in autopsy samples. Clinicians must be mindful of necrotizing pancreatitis in terminal patients.

Identifiants

pubmed: 31688596
doi: 10.1097/MPA.0000000000001423
pii: 00006676-201911000-00015
doi:

Substances chimiques

ACTA2 protein, human 0
Actins 0
Antigens, CD34 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1321-1328

Auteurs

Yoko Matsuda (Y)

From the Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo.
Oncology Pathology, Department of Pathology and Host-Defense, Faculty of Medicine, Kagawa University, Kagawa.

Yoshishige Masuda (Y)

Departments of Infectious Disease.

Keigo Shimoji (K)

Diagnostic Radiology.

Miho Matsukawa (M)

Endoscopy, Tokyo Metropolitan Geriatric Hospital.

Yuko Kinowaki (Y)

Division of Surgical Pathology, Tokyo Medical and Dental University Hospital.

Yuki Fukumura (Y)

Department of Human Pathology, Juntendo University, School of Medicine.

Masataka Kikuyama (M)

Gastrointestinal Division, Komagome Hospital, Tokyo, Japan.

Tomio Arai (T)

From the Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Tokyo.

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Classifications MeSH