WordNet

an abnormal new mass of tissue that serves no purpose (同)tumour, neoplasm

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1. 転移性の胃腸膵管系神経内分泌腫瘍：腫瘍増殖およびホルモン過剰分泌による症状を管理するための局所治療の選択肢 metastatic gastroenteropancreatic neuroendocrine tumors local options to control tumor growth and symptoms of hormone hypersecretion
2. 血管内カテーテル感染症の予防 prevention of intravascular catheter related infections
3. ウィルムス腫瘍の治療および予後 treatment and prognosis of wilms tumor
4. カルチノイド症候群および腫瘍局在の診断 diagnosis of the carcinoid syndrome and tumor localization
5. 気管支神経内分泌（カルチノイド）腫瘍：疫学、危険因子、分類、組織学的検査、診断、および病期分類 bronchial neuroendocrine carcinoid tumors epidemiology risk factors classification histology diagnosis and staging

English Journal

[Amniotic fluid embolism: report of the successful outcome of a case with inaugural cardiac arrest and early DIVC complicated by hemoperitoneum of iatrogen origin and bleeding of an hepatic adenoma].

Falzone E1, Ricard JD, Pachy F, Mandelbrot L, Keïta H.
Annales françaises d'anesthèsie et de rèanimation.Ann Fr Anesth Reanim.2012 Oct;31(10):802-5. doi: 10.1016/j.annfar.2012.07.004. Epub 2012 Aug 24.
Amniotic fluid embolism is a relatively rare clinical entity and with difficult medical recognition. However, it is the second leading cause of maternal mortality. We report here the case of a 32-year-old patient who underwent elective caesarean section complicated by an amniotic fluid embolism with
PMID 22925937

Pulmonary epithelioid hemangioendothelioma.

Rosengarten D1, Kramer MR, Amir G, Fuks L, Berkman N.
The Israel Medical Association journal : IMAJ.Isr Med Assoc J.2011 Nov;13(11):676-9.
Pulmonary epithelioid hemangioendothelioma (PEH), previously known as "intravascular bronchoalveolar tumor," is a rare vascular malignancy with an unpredictable prognosis. Treatment can vary from observation in asymptomatic patients to surgery in patients with resectable disease or chemotherapy in p
PMID 22279701

[A case of intravascular lymphoma with diffuse centrilobular opacities].

Shinoda H1, Maejima A, Shimizu K, Onaka A, Boku T, Oyamada Y.
Nihon Kokyūki Gakkai zasshi = the journal of the Japanese Respiratory Society.Nihon Kokyuki Gakkai Zasshi.2010 Jan;48(1):76-80.
A 54-year-old woman was admitted with general fatigue and dyspnea on exertion. Her serum LDH level was markedly elevated to 2145 IU/L, and chest CT revealed diffuse centrilobular opacities. Total cell counts in bronchoalveolar lavage fluid were elevated, and lymphocytes accounted for 98% of the cell
PMID 20163027

Related Links

Intravascular Bronchioloalveolar Tumor: A Distinctive Surgical ...

alveolar tumor is described, and the clinical and patho- logical characteristics of the tumor are discussed. So-called intravascular bronchioloalveolar tumor (IVBAT) is a relatively new, but well-recognized lung

Intravascular bronchioloalveolar tumour.

Intravascular bronchioloalveolar tumor. Am Rev Respir Dis. 1981 Apr; 123 (4 Pt 1):468–470. [] Farinacci CJ, Blauw AS, Jennings EM. Multifocal pulmonary lesions of possible decidual origin (so-called pulmonary deciduosis): report ...

Intravascular bronchioloalveolar tumor (IV-BAT).

Intravascular bronchioloalveolar tumor (IV-BAT) is a recently described, histologically distinct, malignant, primary lung neoplasm. Originally it was believed to arise from type II alveolar cells which invade blood vessels within the lung, and hence its name.