Cancer Follows Injection of Germ from Proved Case

1933 ◽  
Vol 23 (626) ◽  
pp. 211
Keyword(s):  
1993 ◽  
Vol 161 (1) ◽  
pp. 44-46 ◽  
Author(s):  
J F Gruden ◽  
W R Webb
Keyword(s):  

Author(s):  
P. M. Stockdale

Abstract A description is provided for Nannizzia fulva. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Recorded only from man (but see NOTES). Guinea-pigs have been experimentally infected. DISEASE: Ringworm (dermatophytosis, tinea). Nannizzia fulva is present in the soil and apparently only rarely pathogenic. The scalp (tinea capitis) and glabrous skin (tinea corporis) may be infected. Skin lesions are inflammatory. The only proved case of scalp infection is that recorded by Uriburu (1909); according to Sabouraud (Les Teignes, 1910, p. 241) in this case there was a light inflammatory reaction and infected hairs were indistinguishable from those in M. audouinii infections. In experimental inoculations of guineapigs (Rdzanek, pers. comm.) N. fulva was slightly less virulent than N. gypsea and N. incurvata, the reaction varying from negative to strongly inflammatory. A few ectothrix hyphae breaking up into arthrospores were seen on some hairs, and infected hairs did not fluoresce under Wood's light. GEOGRAPHICAL DISTRIBUTION: Africa (Tanzania), Europe (Great Britain, Hungary, Yugoslavia), South America (Argentina). Probably world-wide in distribution in the soil, but there may be local limiting factors (e.g., in Great Britain it has been recorded only for Bristol, Somerset, and Wiltshire).


Cancer ◽  
1953 ◽  
Vol 6 (3) ◽  
pp. 578-580 ◽  
Author(s):  
Weldon K. Bullock ◽  
Harold L. Thompson ◽  
George Gregory
Keyword(s):  

2008 ◽  
Vol 122 (11) ◽  
Author(s):  
M B Naguib ◽  
N Al-Jazan ◽  
T Hashem

AbstractObjective:We report a histologically proved case of lymphangiomatosis of the skull, involving the temporal bone and presenting as multiple lytic bone lesions.Method:A case report and a review of the literature concerning lymphangiomatosis are presented.Results:Lymphangiomatosis affecting bones is a rare disorder caused by a congenital malformation of the lymphatic system, resulting in diffuse proliferation of the lymphatic channels and involving bones, parenchymal organs and soft tissue. Involved bones show massive osteolysis and progressive, localised bone resorption.Conclusion:Lymphangiomatosis should be kept in mind in the differential diagnosis of lytic lesions of the skull.


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