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thymoma/ateş

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NesneKlinik denemelerPatentler
Sayfa 1 itibaren 85 Sonuçlar

[Thymoma with Hemorrhage and Necrosis Presenting with Fever and Chest Pain;Report of a Case].

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A 53-year-old man was admitted to our hospital for treatment of fever and chest pain. Chest computed tomography showed an anterior mediastinal cystic tumor 39×57 mm in size surrounded by fat with edema and left pleural effusion. After one course of antibiotic administration, the edema of fat

Cytoreductive Pleurectomy and Intra Thoracic Chemo Hyperthermia for Pleural Relapse of Thymomas.

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Several surgical procedures, from debulking to extra pleural pneumonectomy, may be applied for stage IVa Masaoka thymomas but their efficiency is still controversial. Case studies favored R0 resection as the cornerstone of multimodal therapy for loco-regional metastatic extension. We report our

Intra-Thoracic Chemo-Hyperthermia for pleural recurrence of thymoma.

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Pleural recurrences are a hallmark of thymomas, and represent a challenge for multidisciplinary management. The purpose of this study was to assess the feasibility and the results in terms of morbidity, mortality and survival rates, of Intra-Thoracic Chemo-Hyperthermia (ITCH) for the treatment of

Fever of unknown origin caused by intrathyroidal thymic carcinoma.

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Editorial: pleural recurrence of thymoma-what is the value of intra-thoracic chemo-hyperthermia?

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Intra-Thoracic Chemo-Hyperthermia for pleural recurrence of thymomas.

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History of thymoma and yellow fever vaccination.

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Polymyositis associated with thymoma and the subsequent development of pure red cell aplasia.

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A 53-year-old woman with polymyositis associated with thymoma subsequently developed pure red cell aplasia (PRCA). She was hospitalized because of fever and muscle weakness, and diagnosed as having polymyositis by muscle biopsy. Remarkable clinical improvement followed administration of

Complete remission of pure white cell aplasia associated with thymoma after thymectomy and cyclosporine administration.

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We present the case of a 63-year-old male with pure white cell aplasia (PWCA), a rare complication of thymoma, who was successfully treated with cyclosporine A (CyA) and thymectomy. The patient presented with high fever and agranulocytosis. Complete blood count revealed a white blood cell count of

[Recurrence of thymoma accompanied with hypogammaglobulinemia 20 years after surgery: a case report].

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We reported a case of recurrence of localized thymoma accompanied with hypogammaglobulinemia (Good's syndrome) 20 years after surgery. A 74-year-old man was admitted to this hospital because of mediastinal tumor and chronic pulmonary infection. He had been thymectomised at the age of 55 because of

Triad of thymoma, myasthenia gravis and pure red cell aplasia combined with Sjögren's syndrome.

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A 36-year-old woman complained of cough and high fever. Computed tomographic scans demonstrated a mediastinal mass. A couple of months later, she developed dryness in her eyes and mouth. Biopsy of the lip confirmed the diagnosis of Sjögren's syndrome. She underwent thymo-thymomectomy. Pathological

[Hypertrophic osteoarthropathy revealing a malignant thymoma in a child].

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Association of hypertrophic osteoarthropathy and malignant thymoma is very rare in children. Authors report a case of a 14 year old girl followed for rheumatic fever since she was 8 years old. She was explored for arthralgia. The exam showed hippocratic fingers, soft tissues hypertrophy of lower

Minimal-change nephropathy and malignant thymoma.

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A 56-year-old man had fever, precordial pain, and a mediastinal mass. The mass disappeared two months later and the patient remained asymptomatic for 2 1/2 years. At that time a full-blown nephrotic syndrome developed, with minimal-change glomerulopathy. The chest x-ray film showed the reappearance

Disseminated Salmonella Infection Coexisting with Thymoma.

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A 21-year-old boy presented with high grade fever, diffuse chest pain and exertional breathlessness of one month duration. Radiologically he had a large lobulated anterior mediastinal mass with necrotic thick enhancing septaes. Histopathology of the mass was suggestive of thymoma and culture from

[Thymoma in children: a report of one case].

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BACKGROUND Thymoma is an uncommon tumor of childhood. It is an anterior mediastinal tumor with few symptoms. The pleura is the most frequent metastatic site. Surgery is the treatment of choice and the most important prognostic factors are the stage at initial presentation and whether complete
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