Larval Echinococcus multilocularis Leuckart, 1863 in the southern Interlake area in Manitoba

1969 ◽  
Vol 47 (4) ◽  
pp. 733-734 ◽  
Author(s):  
Chiu-Fan Lee

Larval Echinococcus multilocularis was found in one of 25 Peromyscus maniculatus collected in a dolomite quarry near Gunton, about 30 miles north of Winnipeg. This finding shows that E. multilocularis is present in Manitoban rodents at least in an area of 60 sq. mi.

1969 ◽  
Vol 47 (1) ◽  
pp. 135-138 ◽  
Author(s):  
P. D. Leiby ◽  
G. Lubinsky ◽  
W. Galaugher

Cysts of Echinococcus multilocularis Leuck. 1863 were found in 15 of 99 deer mice, Peromyscus maniculatus (Wagner), from a dolomite quarry and a gravel pit 12 and 20 miles north northeast of Winnipeg respectively, in the Stony Mountain – Argyle area. This is the first report on the occurrence of E. multilocularis in Manitoba rodents. It extends northeast the known area of distribution of this cestode in the North American prairies.


1971 ◽  
Vol 49 (4) ◽  
pp. 575-576 ◽  
Author(s):  
John C. Holmes ◽  
Jerome L. Mahrt ◽  
William M. Samuel

Echinococcus multilocularis Leuckart, 1863 has been recovered from 63 of 283 Peromyscus maniculatus trapped near Edmonton, Alberta. This record extends the known distribution of Echinococcus multilocularis in central North America to the northwestern edge of the prairie and into the aspen parkland zone.


1974 ◽  
Vol 52 (8) ◽  
pp. 1091-1091 ◽  
Author(s):  
Gordon A. Chalmers ◽  
Morley W. Barrett

In 1972, cysts of Echinococcus multilocularis were observed in two adult Peromyscus maniculatus trapped within 1.8 km of Lethbridge, Alberta. These findings extended the known distribution of this parasite in Alberta and in southwestern Canada.


2010 ◽  
Vol 34 (8) ◽  
pp. S57-S57
Author(s):  
Jianbing Ding ◽  
Yao Li ◽  
Xu Qi ◽  
Xiumin Ma ◽  
Renyong Lin

2019 ◽  
Vol 98 (4) ◽  
pp. 167-173

Introduction: Alveolar echinococcosis (AE) is a zoonosis caused by Echinococcus multilocularis. AE is primarily localised in the liver. Echinococcus multilocularis imitates tumour-like behaviour. It can metastasise through blood or lymphatic system to distant organs. Echinococcosis often remains asymptomatic due to its long incubation period and indistinct symptoms. Clinical symptoms are determined by the parasite’s location. Diagnosis of echinococcosis is based on medical history, clinical symptoms, laboratory tests, serology results, imaging methods and final histology findings. Surgical removal of the cyst with a safety margin, followed by chemotherapy is the therapeutic method of choice. Case report: We present a case report of alveolar echinococcosis in a thirty-year-old female patient in whom we surgically removed multiple liver foci of alveolar echinococcosis. The disease recurred after two years and required another surgical intervention. Conclusions: Alveolar echinococcosis is a disease with a high potential for a complete cure provided that it is diagnosed early and that the recommended therapeutic procedures are strictly adhered to.


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