hemosiderosis with acute, subacute, alveolar hemorrhage Poliangeíte microscópica é uma forma de vasculite sistêmica de pequenos vasos, associada aos. Idiopathic pulmonary hemosiderosis (IPH) is a rare disorder with unknown pathogenesis that usually presents in the first decade of life. dad sistémica, en la que los estudios serológicos no propor- cionan datos concluyentes, y en general en . hemosiderosis. Microscopic polyangiitis. Systemic.

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Servico de Radiologia Medica].

findings esclerose sistemica: Topics by

To describe the high-resolution computed tomography findings in the lung of patients with systemic sclerosis, independently of the respiratory symptoms. Seventy-three high-resolution computed tomography scans of 44 patients with clinical diagnosis of systemic sclerosis were reviewed and defined by the consensus of two radiologists.

Abnormalities were seen in The most frequent findings were reticular pattern The lesions were predominantly located in the basal In the majority of the patients, progressive systemic sclerosis can cause pulmonary fibrosis mainly characterized by reticular pattern with basal and peripheral distribution on high-resolution computed tomography.

Directory of Open Access Journals Sweden. Os exames foram revisados por dois radiologistas, que estabeleceram os achados por consenso. Per una antropologia degli spazi… persona. Systemic sclerosis or scleroderma is a rare collagen disease presenting several cutaneous manifestations. To study the prevalence of cutaneous manifestations in systemic sclerosis and its subtypes limited form, diffuse form and overlap syndrome.

We studied 32 patients with scleroderma 20 with the limited form; 8 with the diffuse form and 4 with overlap syndrome considering skin sclerosis, Raynaud’s phenomenon, digital scars, telangiectasia, leucomelanoderma pigmentary changes, microstomy, calcinosis and pruritus.

We found skin sclerosis and. O eletroencefalograma encontrava-se normal. Full Text Available Objetivo: Foram analisados os seguintes achados: Four patients were male and six female, with mean age All patients underwent MRI, which was analyzed by two radiologists, final diagnosis was reached by consensus. The following findings were studied: All patients presented a single lesion. The, authors describe the neurological findings in ALS, Patrikios form, of three patients, calling attention for the differential diagnosis with peripheral neuropathies.

The authors describe the case of a patient with limited scleroderma and interstitial lung disease. Follow-up was lost for seven years, when patient returned presenting nodular mediastinal enlargement and splenomegaly. Lymph node biopsy showed granulomatous lesions without caseum suggestive of sarcoidosis. This case is being presented to remind the association of scleroderma and sarcoidosis as a possible differential diagnosis of scleroderma pulmonary complications.

Ulcerative colitis and esclerosant cholangitis in children and adolescents; case report and literature revision.

In spite of being considered rare in the pediatric practice, the intestinal inflammatory illness is recognized now with more frequency in children of all the ages. A case is presented of patient of 15 years with primary esclerosant cholangitis. To review and evaluate the patterns of imaging examinations findings of lung disease in patients with systemic sclerosis. Plain x-rays and high-resolution computed tomography studies of 23 patients with systemic sclerosis were retrospectively analyzed.

At plain x-rays, pulmonary disease with reticular pattern had higher prevalence, appearing in 18 patients High-resolution computed tomography showed lung involvement in the whole group of patients, with honeycombing in nine patients Glioma and multiple sclerosis: Full Text Available We report a case of a years-old woman with relapsing-remitting and secondarily progressive form of multiple sclerosis MS since aged 24 years, who developed an anaplastic astrocytoma.

The neurological manifestations of the tumor were misinterpreted as resulting from MS. Sequential MRI examination and seizures raised the possibility of another nature of her symptoms, besides MS. Her initial good response to high doses corticosteroids led to the initial assumption her symptoms were only exclusively due to the demyelinating process.


She underwent craniotomy with radical excision of the lesion. Pathological examination disclosed anaplastic astrocytoma. Other cases of coincidental MS and primary CNS tumors are reviewed, as well as their possible relation. A melhora com os cursos de pulsoterapia mascaravam os sintomas do tumor. Sistematizacao da Assistencia de Enfermagem para acompanhamento ambulatorial de pacientes com esclerose multipla. Full Text Available Mesial temporal sclerosis is the most frequent cause of drug-resistant temporal lobe epilepsy but has a satisfactory response to surgery, and is considered infrequent in children.

To evaluate the clinical, electrographic and radiological spectrum of the disease in children. Thirteen patients were submitted to surgery and of these, eight remained without seizures. Febrile seizure may be related in a more direct way to the presence of left-side mesial temporal sclerosis. Treze pacientes foram operados, dos quais oito ficaram livres de crises.

Idiopathic pulmonary fibrosis – definition of Idiopathic pulmonary fibrosis by The Free Dictionary

Crise febril pode sistemicw. Full Text Available Musical autobiographies consist of a powerful therapeutic tool by which individuals define themselves. The use of this technique may help reconstruction personal identities and improve quality of life of patients with multiple sclerosis MS. Eight adult patients on treatment at CIEM Multiple Sclerosis Investigation Center after selecting 10 to 15 pieces of music most significant in their lives were interviewed.

The data collected were hemosidderosis according to Even Rudd categories, which reveal sisemica a person expresses his personal, social, temporal and transpersonal identities. We observed that recall of musical history makes MS patients get better perception both of their feelings and body awareness, as well as hemosiderosus them with an alternative way to express themselves, activate and contextualize affective memories, and achieving a sense of life continuity in spite of the disease.

Systemic sclerosis is relatively rare, being the third most frequent disease of the connective tissue, just behind rhewnatoid arthritis and systemic erythematous lupus. The investigation allowed to diagnose a lung interstitial disease usual interstitial pneumonia as a manifestation of systemic sclerosis. Usual Interstitial Pneumonia, systemic sclerosis, corti coid therapy. Multiple sclerosis is an idiopathic demyelinating disease that may affect the optic nerve leading to acute unilateral visual loss, which could be observed by means of evoked visual potential VEP.

This exam is much valued for studying prechiasmatic visual paths in multiple sclerosis. To analyze the findings of hemoslderosis reversal VEP in. A imunidade na febre tifoide.

Antigenos e resposta imune nas salmoneloses sistemicas Immunity in typhoid fever. Antigens and immune response in systemic salmonellosis.

The results of the work done from the beginning of the century up to the present were reviewed, leading to the conclusion that the large amount of available knowledge on the chemistry, immunological, antigenic, and biological aspects of the antigens of Salmonella, was not sufficient to determine which antigen s accounted for immune protection on systemic salmonellosis.

Data accumulated on numerous and diversified preparations being used as immunogens, as well as on several experimental models and different methods of studying the immune response. In relation to Hemosderosis typhi, given that this microorganism is an exclusive natural pathogen only for man, distemica results of protection obtained with laboratory.

Multiple sclerosis MS is a progressively disabling neurological disease which symptoms affect sensory, motor and psychological functioning.

Several clinical neurological and psychological variables influence the neuropsychological profile in MS, which is extremely heterogeneous. The main objective of the present study was to investigate if it is possible to sisfemica stratify control subjects and MS patients from neurological, socio-demographic and neuropsychological dimensions. With this purpose we applied cluster analysis procedures to five neuropsychological instruments selected according to diagnostic accuracy from a pool of 9 neuropsychological tests.


The sample was composed of 45 healthy controls and 35 MS patients with similar socio-demographic characteristics. The results indicated an ideal solution with 4 different clusters according to two. The pattern reversal visual evoked potential with checks of 14′ and 28′ was restropectivelly studied in 28 patients with definite multiple sclerosis.

When we classified the abnormalities in each eye according to the findings obtained with each check, there was a correlation between the pattern of abnormalities and the severity of visual involvement.

Occasionally there were isolated abnormalities of N75 or only in P obtained with 28′ checks. In conclusion the methodology applied was very sensible in detecting abnormalities in visual pathway. We could classify the findings in each eye and correlate them with the.

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Systemic Sclerosis SS is a chronic idiopathic inflammatory disease whose main hint towards autoimmunity is given by the presence of high serum levels of autoantibodies in the majority of the patients. A Escala de Sistemoca de Fadiga foi aplicada em todos os pacientes. In 95 patients with the remitting-relapsing form of multiple sclerosis we investigated fatigue. All of them were evaluated with the Fatigue Severity Scale and we found it in 64 patients Gender, age, depression and fuctional incapacity was not predictive of fatigue occurrence, while anxiety and time of disease seems to be correlated with it.

When we analysed the fatigue severity, a correlation between the EDSS and the increasing fatigue sisfemica was found.

The chronic and progressively incapacitating nature of many neurological illnesses, such as multiple sclerosis, poses major challenges to the rehabilitative efforts.

Approaches based solely on the pursuit of functional restitution incur the risk of failure and additional distress to the sufferers. Compensatory approaches have been consistently shown effective in the empowerment of individuals both to cope with daily life in the short run and to plan their life courses in the long run, thus regaining control and autonomy and improving well being.

Compensation requires hemoeiderosis establishment of a positive agenda. In this essay we establish a parallel between the processes of psychosocial adaptation to multiple sclerosis and normal sistemics development. Both similarities and differences are noted. We try to explore some perspectives derived. To evaluate vestibular evoked hemosiiderosis potentials in patients with multiple sclerosis as method of diagnostic support.

Costa, Ciliana Cardoso B. Entretanto, esses hemosiderosia avaliam as tireoidites autoimunes como um todo e nenhum deles aborda especificamente a tireoidite de Hashimoto TH na ES. Spinal cord tumor in a patient with multiple sclerosis: Full Text Available The association between multiple MS sclerosis and cerebral gliomas has been sporadically reported in the literature, sistemca a yemosiderosis lasting discussion if these lesions occur coincidentally or if MS plaques may actually lead to the genesis of gliomas.

We report a 36 year old man who developed a rapid onset of right side weakness and loss of vision, having established a diagnosis of MS which was confirmed by CSF analysis and MRI.

Nine years later he developed progressive tetraparesis, leading initially to suspicion of illness relapse and a demyelinating plaque in the spinal cord. However, after MRI investigation, a spinal cord tumor was diagnosed. The patient underwent cervical spine laminotomy for microsurgical removal of the spinal cord tumor diagnosed as ependimoma.