Base de dados : HANSEN
Pesquisa : DIAGNOSTICO DIFERENCIAL [Descritor de assunto]
Referências encontradas : 167 [refinar]
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  1 / 167 HANSEN  
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Id:25257
Autor:Mak, Donna B; Platt, Eleanor M; Heath, Christopher H
Título:Leprosy transmission in the Kimberley, Western Australia: still a reality in 21st-century Australia
..-
Fonte:s.l; s.n; 2003. 1 p. .
Descritores:HANSENIASE/epidemiol
HANSENIASE/prev
HANSENIASE/transm
AUSTRALIA OCIDENTAL/epidemiol
QUALIDADE DOS CUIDADOS DE SAUDE/tend
QUALIDADE DOS CUIDADOS DE SAUDE/util
COMPETÊNCIA CLINICA
 DIAGNOSTICO CLINICO
 DIAGNOSTICO DIFERENCIAL
 DIAGNOSTICO DA SITUACAO DE SAUDE EM GRUPOS ESPECIFICOS
Limites:HUMANO
Adolescente
Localização:BR191.1; 01072/s


  2 / 167 HANSEN  
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Id:24809
Autor:William B Reed; Anker K Jensen; B E Konwaler
Título:The cutaneous manifestations in wegeners granulomatosis
ver-
Fonte:California; s.n; 1963. 15 p. ilus.
Resumo:Wegeners granulomatosis is a rare puzzling disease generally characterized by necrotizing granulomatous lesions in the lungs and upper respiratory tract generalized necrotising vasculitis and acute glomerulitis Pathologically tehre is focal necrotizing vasculitis involving the small arteries and veins of the respiratory tract as well as those of the kidney spleen heart intestines liver mucous membranes and skin. In this rport we wish to stress that the cutaneous manifestations are often a prominent feature of wegeners granulomatosis and occasionally are the first sign of the desease. The basis for this report is II8 patients with unequivocal wegener granulomatosis screened from the word literature. The authors cheched al the reported cases of wegeners granulomatosis as well as the conditions frequently confused with it such as periarteritis nodosa lethal medline granuloma the stevens johson syndrome and several others. With but few exceptions patientes were included in this series only if an apparent diagnosis of wegeners granulomatosis was confirmed by gross autopsy examination or by microscopy biopsy examination using the widely accepted pathologic criteria of Godman and Churg (2). If there were any doubt about the diagnosis in any patient in any series or if the pathologic evidence were only presumptive that patient wasexcluded from this study. Our object was to review as many patients as possiblewith clear cut wegeners granulomatosis in order to study the extent of the cutaneos involvement in this disease. In addition to illustrate some of the problems inherent in distinguishing wegener granulomatosis from other conditions characterized by necrotizing angiitis with granuloma we have included five cases form our personal experience. All of these had mucosal lesions and four of the five had atypical pneumonias. Autopsy examination of the four who have died indicated that there had authentic wegeners granulomatosis while the evidence in the other two patients suggests their condition possibily could be due to this entity yet there are many atypical features that cast doubt on the diagnosis. (AU).
Descritores:GRANULOMATOSE DE WEGENER/compl
GRANULOMATOSE DE WEGENER/diag
GRANULOMATOSE DE WEGENER/patol
GRANULOMATOSE DE WEGENER/fisiopatol
DIAGNOSTICO DIFERENCIAL
 MANIFESTAÇÕES CUTANEAS
Limites:HUMANO
Localização:BR191.1; 01164/s


  3 / 167 HANSEN  
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Id:23186
Autor:Boggild, Andrea K; Keystone, Jay S; Kain, Kevin C
Título:Leprosy: a primer for Canadian physicians
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Fonte:s.l; s.n; Jan. 2004. 8 p. ilus, tab.
Resumo:Leprosy is a rare but serious infectious disease caused by Mycobacterium leprae. While global prevalence of the disease is decreasing, increasing rates of immigration from countries where leprosy is endemic have led to the recognition of this illness in North America. Classically, leprosy presents as hypopigmented cutaneous macules along with sensory and motor peripheral neuropathies, although the clinical manifestations vary along a disease spectrum. In addition to primary infection, patients may undergo a [quot ]reaction,[quot ] an acute inflammatory response to the mycobacterium, which leads to pain and erythema of skin lesions and dangerous neuritis. Reactions can occur at any time during the course of leprosy, but they tend to be precipitated by treatment. They are a significant cause of impaired quality of life due to marked nerve damage and thus warrant prompt intervention. Although leprosy may have a protracted onset and be difficult to recognize, cure is achievable with appropriate multidrug therapy. Because untreated leprosy can result in permanent, irreversible nerve damage and secondary transmission, early diagnosis and treatment are essential to minimize morbidity. (AU).
Descritores:Diagnóstico Diferencial
Hanseníase/*/CL/DI/EP/TH
Prognóstico
Limites:HUMANO
Localização:BR191.1; 09330/s


  4 / 167 HANSEN  
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Id:22733
Autor:Grimald, J; Vallat, J. M
Título:Manifestations neurologiques de la lepre
Neurological manifestations of leprosy-
Fonte:s.l; s.n; 2003. 19 p. .
Resumo:Leprosy, also known as Hansen's disease, is a chronic, infectious disease caused by Mycobacterium leprae. Bacilli localize preferentially in the skin and peripheral nerves and have a propensity to cause nerve damage. The resulting disability has caused great suffering for victims in many countries. Despite recent advances in the immunopathogenesis, epidemiology and prognostic factors of leprosy nerve damage, many aspects of the disease have remained enigmatic. The spectrum of clinical and pathological manifestations of the disease ranges from lepromatous to tuberculoid, depending on the host's T-cell-mediated immune response. Diagnosis is based on three criteria: characteristic skin lesions in association with thickened nerves, demonstration of acid fast bacilli in slit skin smears, and histopathology of skin biopsies. Nerve biopsy is necessary to establish the diagnosis of pure "neural leprosy". In developed countries, the diagnosis is suspected when a patient who has stayed in an endemic area suffers from a peripheral neuropathy of unknown etiology. To facilitate determination of the appropriate antibiotic regimen, patients are classified as either paucibacillary or multibacillary. Some patients may have multibacillary leprosy in nerves and paucibacillary leprosy in skin, which emphasizes the usefulness of nerve biopsy. The course of the disease is often complicated by immune mediated "reactions", which can rapidly lead to further nerve damage, namely reversal reaction and erythema nodosum leprosy. However, nerves are often functionally impaired before developing obvious symptoms such as skin reactions or nevralgia (silent neuropathy). Early recognition and prompt treatment with corticosteroids of leprous reactions and "silent neuropathies" is very important to prevent disability with all its attendant problems. Research progress from clinical trials may improve current methods of prevention and treatment of nerve damage in leprosy.(AU).
Descritores:Antiinfecciosos/TU
Biópsia
Diagnóstico Diferencial
Hanseníase/DT/*PA/VI
Mycobacterium leprae/IP
Nervos Periféricos/*PA/VI
Pele/VI
Limites:Humano
Localização:BR191.1; 00254/s


  5 / 167 HANSEN  
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Id:22686
Autor:Osaki, Mitsuhiko; Adachi, Hironobu; Gomyo, Yoshihito; Yoshida, Haruhiko; Ito, Hisao
Título:Detection of mycobacterial DNA in formalin-fixed, paraffin-embedded tissue specimens by duplex polymerase chain reaction: application to histopathologic diagnosis
..-
Fonte:s.l; s.n; 1997. 6 p. ilus, tab.
Resumo:Granuloma is a chronic inflammatory process associated with noninfectious agents or infectious diseases such as tuberculosis. Determination of the causative agent might be occasionally difficult in histopathologic sections. In this study, we examined 60 specimens of granuloma or inflammatory lesions that were originally diagnosed as 51 cases of granulomatous inflammation, 6 of leprosy, and 3 of atypical mycobacteriosis. The diagnoses in the last two categories were made both histologically and clinically. All of the sections and DNA were prepared from formalin-fixed, paraffin-embedded blocks. Histopathologic and immunohistochemical findings were compared with the results of duplex polymerase chain reaction (PCR) using two primers to amplify mycobacterial-common 383-base pair (bp) DNA and Mycobacterium tuberculosis-complex-specific 240-bp DNA. Six samples of leprosy and three of atypical mycobacteriosis showed the 383-bp but not the 240-bp band. Among the 51 specimens of granulomatous inflammations, nine showed no band of even the beta-globin, the cases being excluded from this analysis. The 42 specimens of granulomatous inflammation were subdivided into three categories by PCR: (1) 383- and 240-bp positive; (2) 383-bp positive and 240-bp negative; and (3) both negative. Category 1 included 32 specimens (76.2%), being considered as tuberculosis. One specimen was classified into Category 2, indicating possible atypical mycobacterium. Category 3 included nine specimens, composed of five of sarcoidosis and four other agent-induced granulomas, when compared with histologic and clinical findings. These findings indicate that the PCR assay using DNA extracted from paraffin-embedded materials provides useful information to differentiate tuberculosis from other type of granulomas. (AU).
Descritores:Primers do DNA
DNA Bacteriano/*AN
Diagnóstico Diferencial
Fixadores
Formaldeído
Granuloma/*DI
Micobactérias Atípicas/GE
Mycobacterium/*GE
Mycobacterium leprae/GE
Mycobacterium tuberculosis/GE
Inclusão em Parafina
Reação em Cadeia da Polimerase
Tuberculose/*DI
Limites:Humano
Localização:BR191.1; 09184/s


  6 / 167 HANSEN  
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Id:22287
Autor:S. B. B. M. Dharmendra; Chatterji, S. N.
Título:Trigeminal neuritis simulating leprosy.
Fonte:Lepr Ind;17(2):40-42, apr., 1945. ilus.
Descritores:HANSENIASE/compl
HANSENIASE/diag
DIAGNOSTICO DIFERENCIAL
Localização:BR191.1


  7 / 167 HANSEN  
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Id:21786
Autor:Mukerjee, N.
Título:A case of von recklinghausen´s disease with marked thickening of nerves.
Fonte:Lepr Ind;18(2):71-72, apr,. 1946. .
Descritores:HANSENIASE/diag
NEUROFIBROMATOSE 1/diag
DIAGNOSTICO DIFERENCIAL
Limites:RELATO DE CASO
Localização:BR191.1


  8 / 167 HANSEN  
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Id:21589
Autor:Muir, E.
Título:Correspondence (Pseudo-Raynaud's disease in leprosy).
Fonte:Int. J. Lepr;8(2):221-222, Apr.-Jun. 1940. .
Descritores:HANSENIASE/diag
DOENCA DE RAYNAUD
DIAGNOSTICO DIFERENCIAL
Localização:BR191.1


  9 / 167 HANSEN  
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Id:21585
Autor:Pinkerton, Forrest J.
Título:Leprosy of the upper respiratory tract: discussion of early and moderately advanced cases.
Fonte:Int. J. Lepr;8(2):193-206, Apr.-Jun. 1940. .
Descritores:HANSENIASE/compl
HANSENIASE/patol
MUCOSA RESPIRATORIA/microbiol
MUCOSA RESPIRATORIA/patol
MUCOSA RESPIRATORIA/fisiopatol
HANSENIASE/diag
 DIAGNOSTICO DIFERENCIAL
Limites:HUMANO
Localização:BR191.1


  10 / 167 HANSEN  
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Id:21510
Autor:Germond, R. C.
Título:The differential diagnosis of circinate tuberculoid leprides and polycyclic syphilides.
Fonte:Int. J. Lepr;7(3):361-363, July-Sept. 1939. .
Descritores:HANSENIASE TUBERCULOIDE/clas
HANSENIASE TUBERCULOIDE/diag
HANSENIASE
SIFILIS
 DIAGNOSTICO DIFERENCIAL
Localização:BR191.1


  11 / 167 HANSEN  
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Id:21375
Autor:Chatterji, S. N.
Título:Filarial manifestations simulating leprosy.
Fonte:Int. J. Lepr;6(1):74-76, Jan.-Mar. 1938. ilus.
Descritores:HANSENIASE
HANSENIASE/diag
ELEFANTIASE FILARIAL/diag
DIAGNOSTICO DIFERENCIAL
Meio Eletrônico: - .
Localização:BR191.1


  12 / 167 HANSEN  
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Id:21211
Autor:Dharmendra, S. B. B. M.
Título:Leprosy and dermal leishmaniasis.
Fonte:Lepr Ind;12(1):4-10, jan., 1940. ilus.
Resumo:I. The close similarity of lesions of dermal leishmaniasis with certain lesions of leprosy has been brought out 2. The points of defferential diagnosis between the two diseases have been discussed 3. the possibility of the co-existence of both the diseases in the same patient has been pointed out and the importance of a thorough examination of the patient has been stressed 4. Findings in four interesting cases are reported. In one case the patient was referred to this department as a case of leprosy but was found to be suffering only from dermal leishmaniasis. The other three patients came for teatment of leprosy but a thorough axamination revealed the presence of dermal leishmaniasis in addition.
Descritores:HANSENIASE/compl
HANSENIASE/diag
HANSENIASE/fisiopatol
LEISHMANIOSE/sangue
LEISHMANIOSE/diag
DIAGNOSTICO DIFERENCIAL
Localização:BR191.1


  13 / 167 HANSEN  
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Id:21160
Autor:Gupta, K. K.
Título:A case of pellagra simulating leprosy.
Fonte:Lepr Ind;10(2):70-71, apr., 1938. ilus.
Descritores:PELAGRA
HANSENIASE/diag
DIAGNOSTICO DIFERENCIAL
Localização:BR191.1


  14 / 167 HANSEN  
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Id:21136
Autor:Lowe, J.
Título:Leishmania infections of the skin and leprosy.
Fonte:Lepr Ind;9(3):109-110, July, 1937. .
Descritores:HANSENIASE/diag
LEISHMANIOSE/diag
DIAGNOSTICO DIFERENCIAL
Localização:BR191.1


  15 / 167 HANSEN  
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Id:21111
Autor:Chatterji, S. N; Lowe, J.
Título:Some couses other than leprosy of loss of skin sensation, paralysis, and deformity.
Fonte:Lepr Ind;8(4):141-l46, oct., 1936. ilus.
Descritores:HANSENIASE/compl
HANSENIASE/diag
DIAGNOSTICO DIFERENCIAL
Localização:BR191.1


  16 / 167 HANSEN  
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Id:20848
Autor:Satra, I.
Título:Notes on yaws cases in the Mayurbhan.
Fonte:Lepr Ind;5(3):166-167, july, 1933. ilus.
Descritores:HANSENIASE
DIAGNOSTICO DIFERENCIAL
INFECCOES POR TREPONEMA
Localização:BR191.1


  17 / 167 HANSEN  
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Id:20770
Autor:Shelleh, Hamdi H; Al-Shayeb, Abdul M; Khan, Sarosh A; Khan, Latif A; Al-Hateeti, Hussni S
Título:Cold cellulitis: an unusual presentation of leprosy
..-
Fonte:s.l; s.n; 2001. 2 p. ilus.
Resumo:The presentation of leprosy plays an important role in it´s identification. The features of the disease determine how it is clinically approached and diagnosed. Leprosy has diverse types of presentations. They are commonly calm and insidious.(AU).
Descritores:DOENCA AGUDA
BIOPSIA
CELULITE/diag
CELULITE/etiol
DIAGNOSTICO DIFERENCIAL
DERMATOSES FACIAIS/diag
DERMATOSES FACIAIS/etiol
INDIA/etnol
HANSENIASE DIMORFA/compl
HANSENIASE DIMORFA/diag
HANSENIASE DIMORFA/quimioter
HANSENIASE DIMORFA/etnol
DISTRIBUICAO ESPACIAL
Limites:RELATO DE CASO
HUMANO
MASCULINO
ADULTO
Meio Eletrônico: - .
Localização:BR191.1; 09105/s


  18 / 167 HANSEN  
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Id:20744
Autor:Anon.
Título:Editorial notes.
Fonte:Lepr Ind;3(3):97-98, july. 1931. .
Descritores:HANSENIASE/clas
HANSENIASE/diag
DIAGNOSTICO DIFERENCIAL
EDUCACAO
Localização:BR191.1


  19 / 167 HANSEN  
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Id:20740
Autor:Chatterji, S. N.
Título:Dermal leishmaniosis.
Fonte:Lepr Ind;3(3):99-108, july. 1931. ilus.
Descritores:HANSENIASE/diag
LEISHMANIOSE/clas
LEISHMANIOSE/compl
LEISHMANIOSE/diag
LEISHMANIOSE/quimioter
DIAGNOSTICO DIFERENCIAL
Limites:HUMANO
Localização:BR191.1


  20 / 167 HANSEN  
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Id:20707
Autor:Wardman.
Título:A case simultating leprosy Seen on march 17th, 1930.
Fonte:Lepr Ind;2(3):118-20, july. 1930. ilus.
Descritores:HANSENIASE/diag
DIAGNOSTICO DIFERENCIAL
Localização:BR191.1



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