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[Mediastinal leiomyosarcoma]. (纵隔平滑肌肉瘤)。
Pub Date : 2020-02-07 DOI: 10.32388/af52dw
B. C. Steen, S. Flórez Martín, L. Fernández Fáu, J. García Tirado, J. J. Jareño Esteban, J. Ancochea Bermúdez
Primary mediastinal leiomyosarcomas are malignant sarcomas with unknown etiology not deriving from the smooth muscle fiber of the esophagus, trachea or main vessels. Very few cases have been reported in the literature and, although they are clinically unspecific, their histology is unique. The case described here is a 66-year-old woman with a leiomyosarcoma localized at the medium and posterior mediastinum, clinically presented as a mediastinal emergency.
原发性纵隔平滑肌肉瘤是一种病因不明的恶性肉瘤,并非来源于食道、气管或主要血管的平滑肌纤维。文献中报道的病例很少,尽管它们在临床上不具特异性,但其组织学是独特的。这里描述的病例是一名66岁的女性,患有局限于中纵隔和后纵隔的平滑肌肉瘤,临床表现为纵隔急诊。
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引用次数: 3
[Mantle cell lymphoma]. [套细胞淋巴瘤]。
Pub Date : 2020-02-07 DOI: 10.32388/a6i1f3
P. Khosravi Shahi, A. del Castillo Rueda, G. Pérez Manga
Mantle cell lymphoma accounts for approximately 7% of adult Non-Hodgkin Lymphomas. It is a neoplasm of monomorphous small to medium-sized B cells with irregular nuclei. The tumor cells express strong IgM and IgD, and B-cell-associated antigens. Nuclear cyclin D1 protein is present in all cases and is the gold standard for the diagnosis. The t(11;14) (q13;q32) in the majority of the cases results in rearrangement of the BCL-1 locus and overexpression of the cyclin D1 gene. Most patients present with disseminated disease. Mantle cell lymphoma is an incurable neoplasm, but it may be treated with different chemotherapy regimen (R-Hyper-CVAD, R-CHOP, bortezomib) and young patients should be considered for high-dose therapy and autologous or allogeneic bone marrow transplantation.
套细胞淋巴瘤约占成人非霍奇金淋巴瘤的7%。它是一种具有不规则细胞核的单形态中小型B细胞的肿瘤。肿瘤细胞表达强IgM和IgD以及B细胞相关抗原。核细胞周期蛋白D1蛋白存在于所有病例中,是诊断的金标准。在大多数病例中,t(11;14)(q13;q32)导致BCL-1基因座的重排和细胞周期蛋白D1基因的过度表达。大多数患者表现为播散性疾病。Mantle细胞淋巴瘤是一种无法治愈的肿瘤,但它可以用不同的化疗方案(R-Hyper-CVAD、R-CHOP、硼替佐米)进行治疗,年轻患者应考虑进行高剂量治疗和自体或异基因骨髓移植。
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引用次数: 4
[The neuroleptic malignant syndrome]. [抗精神病药物恶性综合征]。
Pub Date : 2020-02-07 DOI: 10.32388/bdk2dh
J. Garćia Castaño, M. García Román, B. Pinilla Llorente, C. Gilsanz Fernández
Dear Editor, The clinical features of an uncommon hypersensitivity to neurolepitcs were first described by Preston, 1 and was subsequently known as neuroleptic malignant syndrome (NMS). The incidence of NMS report elsewhere is between 0.07% 2 7 and the mortality rate is up to 25%. 8, 9 The condition appears to be an idiosyncratic reaction to a therapeutic dose of the antipsychotic drugs especially dopamine receptor antagonists and a dose relationship has been postulated. 10, 11 Despite the sporadic occurrence of NMS in our psychiatric units, no case has been reported from Nigeria. A 21-year-old female nurse who was Gravida 1, Para 1+ developed acute postpartum psychosis of manic type, two days following childbirth. She developed the psychosis on a background of normal personality and absence of any family history of psychiatric or neurological illness. She was initially admitted at a general hospital, where she works. On admission, she was given massive dose of chlorpromazine and paraldehyde intramuscularly (the relations could not ascertain the amount of dosage given). On the third day of admission, she became more restless, confused, pyrexic and developed generalized stiffness. She was transferred to another hospital where a lumbar puncture was done to exclude meningitis, but the cerebrospinal fluid was normal. She was then referred for electroencephalogram (EEG) to exclude organic brain disease. By the time the patient was brought to the EEG clinic, her temperature was 42c and she had marked body rigidity of plastic type with occasional choreoform movement of the limbs and in addition was comatose. Pulse rate was 110 per minute, regular and normal volume and blood pressure 140/95mmHg. The EEG showed diffuse mixture of fast and slow waves and the background activity consisted of muscle artifact on all channels and NMS was suspected. Blood samples were taken for complete blood count, serum electrolytes and urea, liver function tests and serum creatine kinase. All neuroleptic drugs were discontinued and she was moved into an airconditioned room and tepid sponged with water. Bromocriptine was commenced (10mg 6 hourly) along with 10mg diazepam 6 hourly and benzhexol 5mg 8 hourly. All the medications were given intramuscularly for the first 48 hours and orally by nasogastric tube. By the second temperature dropped to 37.5c, blood pressure remained 140/90 mmHg and level of consciousness improved. By this time laboratory results became available; haemogram was 11.5g/dl, white cell count 11.3 x 10/L; serum sodium was 140mmol/l, potassium 6.0mmoI/l, urea 20mg%, aspertate transaminase 50 iu/l, erythrocyte sedimentation rate 22mm/hr and creatine kinase 3600 iu/l. On the 4 day, temperature was normal, and she could recognize familiar people and was able to speak. Her body rigidity became less and she was able to walk with some help. By the 7 day, the patient started becoming restless and talkative, as a result she was placed on thioridazine 100mg 12 hourly
尊敬的编辑,一种罕见的神经安定药超敏反应的临床特征首先由Preston, 1描述,随后被称为神经安定药恶性综合征(NMS)。其他地区报告的NMS发病率在0.07%之间27,死亡率高达25%。8,9这种情况似乎是对治疗剂量的抗精神病药物,特别是多巴胺受体拮抗剂的特殊反应,并且已经假设了剂量关系。10,11尽管在我们的精神科病房有零星发生NMS,但尼日利亚没有报告任何病例。一名21岁女护士,妊娠1期,Para 1+,在分娩后2天出现急性产后躁狂型精神病。她在人格正常的背景下发展为精神病,没有任何精神或神经疾病的家族史。她最初住进了她工作的一家综合医院。入院时给予大剂量氯丙嗪和丙二醛肌注(两者关系无法确定给药量)。入院第三天,患者变得焦躁不安、神志不清、发热并出现全身僵硬。她被转移到另一家医院,在那里做了腰椎穿刺以排除脑膜炎,但脑脊液正常。随后进行脑电图检查以排除器质性脑疾病。当患者被带到脑电图诊所时,她的体温为42℃,她有明显的塑性型身体僵硬,偶尔有肢体舞蹈样的运动,并且昏迷。脉搏每分钟110次,正常和正常体积,血压140/95mmHg。脑电图呈弥漫性快、慢波混合,背景活动在各通道均有肌肉伪影,疑似NMS。采集血样进行全血细胞计数、血清电解质和尿素、肝功能和血清肌酸激酶检测。所有的抗精神病药物都被停用,她被转移到一个有空调的房间,用温水擦拭。溴隐亭开始治疗(10mg 6小时),地西泮10mg 6小时,苯醚索5mg 8小时。所有药物在最初48小时内肌注,然后经鼻胃管口服。第二次体温降至37.5℃时,血压保持在140/90毫米汞柱,意识水平有所改善。这时实验室的结果出来了;血象11.5g/dl,白细胞计数11.3 × 10/L;血清钠140mmol/l,钾6.0 mmol/l,尿素20mg%,谷草转氨酶50iu /l,红细胞沉降22mm/hr,肌酸激酶3600iu /l。第4天,体温正常,能认出熟悉的人,会说话。她的身体变得不那么僵硬了,在一些帮助下她可以走路了。到第7天,患者开始变得焦躁不安和健谈,因此她被放置在硫硝嗪100mg 12小时。她的身体和精神状况持续改善,到第三周时,她已经足够好了,出院时服用噻嗪100mg bd。她一直很好,现在有4个可爱的孩子。临床表现为高热,全身僵硬伴肢体舞蹈样运动,创造激酶升高,大量摄入抗精神病药后出现酸中毒,与其他文献报道的NMS诊断一致。异常脑电图的存在是支持我们诊断的额外发现。由于在我们的环境中难以获得丹trolene等药物,我们采用了一种改良形式的温水海绵,以帮助降低体温,我们提倡使用这种程序,特别是在非洲地区等困难的环境中。试图通过使用苯二氮卓类药物和抗胆碱能药物来减少肌肉僵硬,这些药物在我们的环境中很容易获得。选择硫噻嗪治疗她的精神病状态主要是因为其抗胆碱能的优势,而苯并唑的加入促进了这一优势。正如治疗结果所示,我们认为这种组合比我们可用的其他精神药物相对安全。
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引用次数: 0
[Microscopic polyarteritis]. [显微镜下多动脉炎]。
Pub Date : 2020-02-07 DOI: 10.1007/springerreference_39113
C. L. de Ancos Aracil, J. R. Rebollar Mesa
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引用次数: 2
Chronic fatigue syndrome 慢性疲劳综合症
Pub Date : 2009-01-01 DOI: 10.1007/978-0-387-87687-0_21
M. Garralda
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引用次数: 0
[Giant cell arteritis: and uncommon cause of chronic cough]. 巨细胞动脉炎:慢性咳嗽的罕见病因。
Pub Date : 2008-07-01 DOI: 10.4321/s0212-71992008000700020
M A Sancho Zamora, L M González López, M A Martínez García, A M Puig Rullán
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引用次数: 0
[Diagnosis of the spontaneous subarachnoid hemorrhage with short bleeding or long evolution: report of one case]. 自发性蛛网膜下腔出血短出血或长出血的诊断:附1例报告。
Pub Date : 2008-07-01 DOI: 10.4321/s0212-71992008000700008
E Alonso Formento, F Rodero Alvarez, C M Ros Tristán, M J Calpe Gil, A Martínez Oviedo

Subarachnoid hemorrhage implies the presence of blood within the subarachnoid space from some pathologic process. The initial study of choice is an urgent Cranial Computed Tomography scan, but its sensitivity declines with time. So that it is recommended that patients with severe sudden headache but normal Cranial Computed Tomography scan, should have a lumbar puncture performed, more than 12 hours after the onset of symptoms, to rule out subarachnoid hemorrhage. The methods for distinguishing among traumatic lumbar puncture and true Subarachnoid hemorrhage include the erythrocyte level, the "three tube test", D-dimer assay and ferritin in cerebrospinal fluid. But the best technique is the xanthochromia o yellow-to-orange cerebrospinal fluid supernatant, measured spectrographically. We report a case of a young woman with a subarachnoid hemorrhage diagnosed by xanthochromia after 18 days after the onset of bleeding.

蛛网膜下腔出血是由于某种病理过程导致的蛛网膜下腔出血。最初的研究选择是紧急的颅脑ct扫描,但其灵敏度随时间而下降。因此,建议严重突发性头痛但颅ct扫描正常的患者,应在出现症状12小时以上行腰椎穿刺,以排除蛛网膜下腔出血。鉴别外伤性腰椎穿刺与真性蛛网膜下腔出血的方法包括红细胞水平、“三管试验”、d -二聚体测定和脑脊液铁蛋白测定。但最好的技术是黄到橙的脑脊液上清,用光谱法测量。我们报告一个病例的年轻女性蛛网膜下腔出血诊断为黄色症后18天出血的发作。
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引用次数: 0
[Severe ocular symptoms as an initial manifestation of superior vena cava syndrome]. [严重的眼部症状是上腔静脉综合征的最初表现]。
Pub Date : 2008-07-01 DOI: 10.4321/s0212-71992008000700009
J Barquero-Romero, V López Cupido, O Torrado Sierra, M Valencia Terrón

Superior vena cava syndrome is obstruction of blood flow through the superior vena cava (SVC). It is most commonly caused by neoplasm, especially lung cancer. An obstructed SVC initiates collateral venous return to the heart from the upper half of the body and the classic symptoms and signs become obvious. Superior vena cava síndrome is a rare cause of ocular manifestations. We report a case of periorbital swelling, conjunctival edema an orbital proptosis in a male patient presenting malignant superior vena cava obstruction.

上腔静脉综合征是血液通过上腔静脉(SVC)的阻塞。它最常由肿瘤引起,尤其是肺癌。阻塞的SVC启动侧静脉从上半身返回心脏,典型的症状和体征变得明显。上腔静脉síndrome是一种罕见的眼部表现。我们报告一例眼眶周围肿胀,结膜水肿和眼眶突出的男性患者表现为恶性上腔静脉阻塞。
{"title":"[Severe ocular symptoms as an initial manifestation of superior vena cava syndrome].","authors":"J Barquero-Romero,&nbsp;V López Cupido,&nbsp;O Torrado Sierra,&nbsp;M Valencia Terrón","doi":"10.4321/s0212-71992008000700009","DOIUrl":"https://doi.org/10.4321/s0212-71992008000700009","url":null,"abstract":"<p><p>Superior vena cava syndrome is obstruction of blood flow through the superior vena cava (SVC). It is most commonly caused by neoplasm, especially lung cancer. An obstructed SVC initiates collateral venous return to the heart from the upper half of the body and the classic symptoms and signs become obvious. Superior vena cava síndrome is a rare cause of ocular manifestations. We report a case of periorbital swelling, conjunctival edema an orbital proptosis in a male patient presenting malignant superior vena cava obstruction.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2008-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28051531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
[Autoimmune pancreatitis. Related to a case]. 自身免疫性胰腺炎。与案件有关]。
Pub Date : 2008-07-01 DOI: 10.4321/s0212-71992008000700010
A Villalobos Sánchez, A Muñoz Morente, I Pérez de Pedro, A Navarro Piñero, J M Reguera Iglesias, R Gómez Huelgas

Autoimmune pancreatitis is an entity that has recently been included in the differential diagnosis of chronic pancreatitis-pancreatic mass. The presence of diffuse, irregular Wirsung's duct stenosis, together with high levels of IgG4, the existence of certain autoantibodies and lymphoplasmacytic infiltration of the pancreas are key factors in the diagnosis. An early diagnostic suspicion and multidisciplinary collaboration are vital in these cases to avoid unnecessary surgery as the differential diagnosis is established with such entities as pancreas cancer, chronic pancreatitis, primary biliary cirrhosis or primary sclerosing cholangitis. Autoimmune pancreatitis has an excellent response to steroid therapy, with complete resolution of clinical, analytical and radiological parameters, as occurred in our patient. The very few cases reported so far suggest the need for the elaboration of long-term follow-up studies to determine the prognosis and frequency of its association with other diseases.

自身免疫性胰腺炎是最近被纳入慢性胰腺炎-胰腺肿块鉴别诊断的一个实体。弥漫性不规则Wirsung管狭窄,IgG4水平高,存在某些自身抗体和胰腺淋巴浆细胞浸润是诊断的关键因素。在这些病例中,早期诊断怀疑和多学科合作是至关重要的,以避免不必要的手术,因为胰腺癌、慢性胰腺炎、原发性胆汁性肝硬化或原发性硬化性胆管炎等实体已建立鉴别诊断。自身免疫性胰腺炎对类固醇治疗有很好的反应,临床、分析和放射学参数完全解决,正如本例患者所发生的那样。迄今为止报告的病例很少,这表明需要进行长期随访研究,以确定其与其他疾病的预后和关联频率。
{"title":"[Autoimmune pancreatitis. Related to a case].","authors":"A Villalobos Sánchez,&nbsp;A Muñoz Morente,&nbsp;I Pérez de Pedro,&nbsp;A Navarro Piñero,&nbsp;J M Reguera Iglesias,&nbsp;R Gómez Huelgas","doi":"10.4321/s0212-71992008000700010","DOIUrl":"https://doi.org/10.4321/s0212-71992008000700010","url":null,"abstract":"<p><p>Autoimmune pancreatitis is an entity that has recently been included in the differential diagnosis of chronic pancreatitis-pancreatic mass. The presence of diffuse, irregular Wirsung's duct stenosis, together with high levels of IgG4, the existence of certain autoantibodies and lymphoplasmacytic infiltration of the pancreas are key factors in the diagnosis. An early diagnostic suspicion and multidisciplinary collaboration are vital in these cases to avoid unnecessary surgery as the differential diagnosis is established with such entities as pancreas cancer, chronic pancreatitis, primary biliary cirrhosis or primary sclerosing cholangitis. Autoimmune pancreatitis has an excellent response to steroid therapy, with complete resolution of clinical, analytical and radiological parameters, as occurred in our patient. The very few cases reported so far suggest the need for the elaboration of long-term follow-up studies to determine the prognosis and frequency of its association with other diseases.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2008-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28051532","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Neoplastic angiogenesis]. 肿瘤血管生成。
Pub Date : 2008-07-01 DOI: 10.4321/s0212-71992008000700012
P Khosravi Shahi, A Del Castillo Rueda, G Pérez Manga

Neoplastic angiogenesis is an essential process in the progressive growth of neoplasms and the production of metastasis. Angiogenesis consists of a series of linked and sequential steps that ultimately leads to the development of a neovascular blood supply to the tumor mass. VEGF has got an essential role in neoplastic angiogenesis, therefore it is an important target in the treatment of neoplasms. Bevacizumab, a humanized monoclonal antibody, inhibits VEGF, and may also improve the delivery of chemotherapy to the tumor mass. Multi-kinase ihibitors (sorafenib and sunitinib) are orally administered small-molecules, that inhibit different receptors (essentials in the neoplastic angiogenesis), such as the VEGFR or PDGFR. These agents are useful in the treatment of advanced renal-cell carcinoma, and are under investigation in several tumors.

肿瘤血管生成是肿瘤进行性生长和发生转移的重要过程。血管生成包括一系列相互联系和顺序的步骤,最终导致肿瘤块的新血管血液供应的发展。VEGF在肿瘤血管生成中具有重要作用,是肿瘤治疗的重要靶点。贝伐单抗是一种人源化单克隆抗体,可以抑制VEGF,也可以改善化疗对肿瘤的递送。多激酶抑制剂(索拉非尼和舒尼替尼)是口服的小分子药物,可抑制不同的受体(肿瘤血管生成中必不可少的受体),如VEGFR或PDGFR。这些药物在晚期肾细胞癌的治疗中是有用的,并且在一些肿瘤中正在研究。
{"title":"[Neoplastic angiogenesis].","authors":"P Khosravi Shahi,&nbsp;A Del Castillo Rueda,&nbsp;G Pérez Manga","doi":"10.4321/s0212-71992008000700012","DOIUrl":"https://doi.org/10.4321/s0212-71992008000700012","url":null,"abstract":"<p><p>Neoplastic angiogenesis is an essential process in the progressive growth of neoplasms and the production of metastasis. Angiogenesis consists of a series of linked and sequential steps that ultimately leads to the development of a neovascular blood supply to the tumor mass. VEGF has got an essential role in neoplastic angiogenesis, therefore it is an important target in the treatment of neoplasms. Bevacizumab, a humanized monoclonal antibody, inhibits VEGF, and may also improve the delivery of chemotherapy to the tumor mass. Multi-kinase ihibitors (sorafenib and sunitinib) are orally administered small-molecules, that inhibit different receptors (essentials in the neoplastic angiogenesis), such as the VEGFR or PDGFR. These agents are useful in the treatment of advanced renal-cell carcinoma, and are under investigation in several tumors.</p>","PeriodicalId":50798,"journal":{"name":"Anales De Medicina Interna","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2008-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"28052040","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Anales De Medicina Interna
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