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[PMID]:29384961
[Au] Autor:Pan X; Dong Y; Yuan T; Yan Y; Tong D
[Ad] Endereço:Department of Radiology.
[Ti] Título:Two cases of hemolymphangioma in the thoracic spinal canal and spinal epidural space on MRI: The first report in the literature.
[So] Source:Medicine (Baltimore);96(52):e9524, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Hemolymphangioma is a rare, noninvasive benign tumor of mesenchymal origin resulting from malformation of vascular and lymphatic vessels. The incidence of hemolymphangioma in the spinal canal is low. PATIENT CONCERNS: This report describes 2 patients with a lesion located in the thoracic spinal canal or spinal epidural space, who were misdiagnosed with suspected meningioma or suspected schwannoma, respectively, based on magnetic resonance imaging (MRI). DIAGNOSES: Hemolymphangioma. INTERVENTIONS: The application of a surgery was designed to treat the 2 patients. OUTCOMES: 2 patients stated that symptoms were improved after the operation. LESSONS: This report should raise awareness among clinicians that careful image analysis and consideration of patient history and pathology is required for accurate differential diagnosis of hemolymphangioma in the spinal canal and spinal epidural space.
[Mh] Termos MeSH primário: Espaço Epidural/patologia
Hemangioma/patologia
Linfangioma/patologia
Canal Vertebral/patologia
Vértebras Torácicas/patologia
[Mh] Termos MeSH secundário: Diagnóstico Diferencial
Feminino
Hemangioma/diagnóstico
Hemangioma/cirurgia
Seres Humanos
Linfangioma/diagnóstico
Imagem por Ressonância Magnética
Masculino
Meia-Idade
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180220
[Lr] Data última revisão:
180220
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180201
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009524


  2 / 3844 MEDLINE  
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[PMID]:29186257
[Au] Autor:Oliveti A; Biasi TB; Funchal GDG
[Ad] Endereço:Medical Academy, Fundação Universidade Regional de Blumenau - Blumenau (SC) Brazil.
[Ti] Título:Lymphangioma secondary to irradiation after mastectomy.
[So] Source:An Bras Dermatol;92(3):395-397, 2017 May-Jun.
[Is] ISSN:1806-4841
[Cp] País de publicação:Brazil
[La] Idioma:eng
[Ab] Resumo:Lymphangioma is a rare benign disease of the lymphatic vessels. Typically, they are primary conditions but may be acquired secondarily, such as those caused by irradiation during radiotherapy for the treatment of breast cancer. The local lymphatic obstruction provoked by irradiation causes the appearance of asymptomatic hyaline vesicles on the irradiated skin. The present report describes a 78-year-old female patient, who initially presented hyaline vesicles that progressed into multiple papules with serous exudation of a yellowish and odorless secretion on the area of chronic radiodermitis in right breast. Despite the rarity of the case, we emphasize the importance of knowledge regarding dermatological disease for early diagnosis and proper medical conduct.
[Mh] Termos MeSH primário: Neoplasias da Mama/radioterapia
Linfangioma/diagnóstico
Neoplasias Induzidas por Radiação/diagnóstico
[Mh] Termos MeSH secundário: Idoso
Neoplasias da Mama/cirurgia
Feminino
Seres Humanos
Linfangioma/etiologia
Mastectomia
[Pt] Tipo de publicação:CASE REPORTS
[Em] Mês de entrada:1801
[Cu] Atualização por classe:180131
[Lr] Data última revisão:
180131
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171130
[St] Status:MEDLINE


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[PMID]:28838528
[Au] Autor:Bansal N; Haidar-El-Atrache S; Walters HL; Kobayashi D
[Ad] Endereço:Division of Pediatric Cardiology, Children's Hospital of Michigan, Detroit, Michigan. Electronic address: nehban@gmail.com.
[Ti] Título:Cardiac Lymphangioma Encasing Right Coronary Artery in an Infant.
[So] Source:Ann Thorac Surg;104(3):e279-e281, 2017 Sep.
[Is] ISSN:1552-6259
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Cardiac lymphangioma is a rare primary benign tumor of the heart. We report a 3-year-old with cystic lymphangioma encasing the right coronary artery. Cardiac magnetic resonance imaging confirmed a intra-pericardial heterogeneous mass measuring 2.6 × 2.4 × 3.9 cm and situated right anterolateral to the ascending aorta and extending into the right atrioventricular groove. Furthermore, the right coronary artery traversed through the center of the mass. Surgical resection, on cardiopulmonary bypass, consisted of excision by skeletonizing the right coronary artery along the length of the mass. The pathology report was consistent with a lymphatic malformation. The postoperative course was uneventful without recurrence at follow-up.
[Mh] Termos MeSH primário: Procedimentos Cirúrgicos Cardíacos/métodos
Vasos Coronários
Neoplasias Cardíacas/diagnóstico
Linfangioma/diagnóstico
[Mh] Termos MeSH secundário: Pré-Escolar
Diagnóstico Diferencial
Ecocardiografia
Feminino
Neoplasias Cardíacas/cirurgia
Seres Humanos
Linfangioma/cirurgia
Imagem Cinética por Ressonância Magnética/métodos
Tomografia Computadorizada por Raios X/métodos
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170914
[Lr] Data última revisão:
170914
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170826
[St] Status:MEDLINE


  4 / 3844 MEDLINE  
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[PMID]:28534344
[Au] Autor:Woo YJ; Kim CY; Sgrignoli B; Yoon JS
[Ad] Endereço:Institute of Vision Research, Department of Ophthalmology, Yonsei University College of Medicine, Seoul, Korea.
[Ti] Título:Orbital Lymphangioma: Characteristics and Treatment Outcomes of 12 Cases.
[So] Source:Korean J Ophthalmol;31(3):194-201, 2017 Jun.
[Is] ISSN:2092-9382
[Cp] País de publicação:Korea (South)
[La] Idioma:eng
[Ab] Resumo:PURPOSE: To report the patient characteristics and treatment outcomes in 12 cases of orbital lymphangioma. METHODS: In this study, orbital lymphangioma was diagnosed based on clinical, radiologic (computed tomography, magnetic resonance imaging), and histologic findings when possible. Patients whose vision was not compromised by orbital lymphangioma, or that did not have increased intraocular pressure (IOP), received oral corticosteroids. Orbital lymphangioma that affected vision or increased IOP was treated by surgery, which included aspiration of blood or partial resection with or without injection of a sclerosant. RESULTS: Four patients without compromised vision responded well to oral corticosteroids. Eight patients with compromised vision underwent some form of surgery. Bleeding recurred in three patients after aspiration of blood and in two after partial resection and intralesional injection of a sclerosant. Overall, five patients were treated successfully by aspiration of blood, intralesional injection of a sclerosant, and application of continuous negative pressure by appropriate drainage. Partial resection was successful in two patients with organized hematoma. CONCLUSIONS: Orbital lymphangioma that does not compromise vision can be treated medically using oral corticosteroids. Patients with threatened vision or elevated IOP due to acute hemorrhage should be treated by aspiration of blood, intralesional injection of a sclerosant, and application of continuous negative pressure. Partial resection may be effective only in patients with organized hematoma.
[Mh] Termos MeSH primário: Linfangioma/diagnóstico
Procedimentos Cirúrgicos Oftalmológicos/métodos
Neoplasias Orbitárias/diagnóstico
[Mh] Termos MeSH secundário: Adolescente
Adulto
Idoso
Criança
Pré-Escolar
Feminino
Seguimentos
Seres Humanos
Lactente
Linfangioma/cirurgia
Imagem por Ressonância Magnética
Masculino
Meia-Idade
Neoplasias Orbitárias/cirurgia
Estudos Retrospectivos
Tomografia Computadorizada por Raios X
Resultado do Tratamento
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171012
[Lr] Data última revisão:
171012
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170524
[St] Status:MEDLINE
[do] DOI:10.3341/kjo.2016.0034


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[PMID]:28358710
[Au] Autor:Patel KC; Kalantzis G; El-Hindy N; Chang BY
[Ad] Endereço:Department of Ophthalmology, Huddersfield Royal Infirmary, Huddersfield, U.K. karnesh@doctors.org.uk.
[Ti] Título:Sclerotherapy for Orbital Lymphangioma - Case Series and Literature Review.
[So] Source:In Vivo;31(2):263-266, 2017 Mar-Apr.
[Is] ISSN:1791-7549
[Cp] País de publicação:Greece
[La] Idioma:eng
[Ab] Resumo:Orbital lymphangioma is a lymphatic system lesion that commonly presents in childhood. Management of these lesions is complex. Sclerotherapy is a therapy used to treat and shrink lesions prior to or as an alternative to surgery. We present three cases of orbital lymphangioma that were treated with sclerotherapy. Case 1: A 6-month-old boy was presented in 2010 with right ptosis and proptosis. Magnetic resonance imaging (MRI) identified a lesion involving the right orbit and face. Case 2: A 3-year-old girl was presented in 2011 with intermittent right periorbital swelling and medial canthal bleeding. MRI identified a soft-tissue lesion in the right orbit, extending into the face. Case 3: A 3-year-old girl was presented in 2012 with vomiting, and painful right proptosis. MRI identified an intra-conal lesion in the right orbit with fluid filled levels. All three patients were treated with sclerotherapy (sodium tetradecylsulfate). Sclerotherapy is a promising treatment for orbital lymphangioma. Its use may prevent the need for, or minimise the amount of surgical management. Several sclerosants are now commonly used to treat these lesions.
[Mh] Termos MeSH primário: Linfangioma/terapia
Neoplasias Orbitárias/terapia
Escleroterapia/métodos
[Mh] Termos MeSH secundário: Pré-Escolar
Feminino
Seres Humanos
Lactente
Linfangioma/diagnóstico por imagem
Imagem por Ressonância Magnética
Masculino
Órbita/diagnóstico por imagem
Órbita/patologia
Neoplasias Orbitárias/diagnóstico por imagem
Soluções Esclerosantes/uso terapêutico
Tetradecilsulfato de Sódio/uso terapêutico
Resultado do Tratamento
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Sclerosing Solutions); Q1SUG5KBD6 (Sodium Tetradecyl Sulfate)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170601
[Lr] Data última revisão:
170601
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170331
[St] Status:MEDLINE


  6 / 3844 MEDLINE  
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[PMID]:28272235
[Au] Autor:Pandey S; Fan M; Zhu J; Lu X; Chang D; Li X
[Ad] Endereço:aDepartment of Radiology bDepartment of Pathology cDepartment of Maternal and Child Health, School of Public Health, Sun Yat-sen University, Guangdong, China.
[Ti] Título:Unusual cause of 55 years of rectal bleeding: hemolymphangioma (a case report).
[So] Source:Medicine (Baltimore);96(10):e6264, 2017 Mar.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Hemolymphangioma is a rare developmental error of combined blood and lymphatic vasculature. To the best of our knowledge, there is only one case of rectal hemolymphangioma reported in Pubmed. Our case probably is the first reported rectal hemolymphangioma with computed tomography (CT) evaluation. PATIENT CONCERNS AND DIAGNOSIS: A 57-year-old male was presented to our hospital with 55 years of long history of episodic rectal bleeding. Past medical history showed numerous hospital visits for similar illness. Multiple diagnoses were made and different treatment modalities were applied for his benefit, but none of them relieved the symptoms permanently. He was then referred to our hospital. On admission, he was presented with intermediate rectal bleeding of fresh blood. CT examination showed isodense homogenous rectal wall thickening with heterogeneous enhancement on contrast examination. Multiple calcifications were seen in and around the lesion. INTERVENTIONS AND OUTCOMES: He underwent open abdominal surgery with total surgical excision of the lesion. Post-surgical histopathological examination of excised specimen showed submucosal multiple thin-walled vessel of varying size, some consistent with blood vessel and other with lymph vessel, thus diagnosis of hemolymphangioma was made. Follow-up for 6 months showed no recurrence. LESSIONS: Hemolymphangioma is a benign developmental lesion. Radiological findings can be challenging and range from benign cystic lesion to aggressive lesion mimicking malignancy. Therefore, combined clinical history, radiological findings, and continuous follow-up can help make proper diagnosis and provide prompt and accurate treatment.
[Mh] Termos MeSH primário: Hemorragia Gastrointestinal/etiologia
Hemangioma/complicações
Linfangioma/complicações
Doenças Retais/etiologia
[Mh] Termos MeSH secundário: Hemangioma/diagnóstico
Hemangioma/cirurgia
Seres Humanos
Linfangioma/diagnóstico
Linfangioma/cirurgia
Masculino
Meia-Idade
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170324
[Lr] Data última revisão:
170324
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170309
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000006264


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[PMID]:28189546
[Au] Autor:Spier AB; Kurtz J; Sears D
[Ad] Endereço:Department of Internal Medicine, Division of Infectious Disease, Harbor-ULCA Medical Center, 1000 West Carson Street, Torrance, CA 90509, United States. Electronic address: aspier@dhs.lacounty.gov.
[Ti] Título:A novel case of lymphangiomatosis in HIV.
[So] Source:Exp Mol Pathol;102(2):251-254, 2017 Apr.
[Is] ISSN:1096-0945
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Diffuse lymphangiomatosis is a rare disorder characterized by abnormal proliferation of lymphatic channels. It can involve just one organ or multiple organs, such as liver, spleen, lungs, and bone. This disorder generally presents in children and young adults, but in rare cases, patients first present with symptoms in adulthood. Here, we describe a 48-year-old HIV-positive man who presented with shortness of breath. Computed tomography scan revealed a large right-sided pleural effusion and a heterogeneously enhancing liver. Thoracentesis demonstrated a chylous effusion and subsequent liver biopsy revealed a proliferation of dilated lymphatics to establish a diagnosis of lymphangiomatosis.
[Mh] Termos MeSH primário: Infecções por HIV/fisiopatologia
Linfangioma/diagnóstico
Linfangioma/fisiopatologia
[Mh] Termos MeSH secundário: Antirreumáticos/uso terapêutico
Bevacizumab/uso terapêutico
Proliferação Celular
Infecções por HIV/tratamento farmacológico
Seres Humanos
Pulmão/patologia
Linfangioma/tratamento farmacológico
Vasos Linfáticos/citologia
Vasos Linfáticos/patologia
Masculino
Meia-Idade
Derrame Pleural/metabolismo
Propranolol/uso terapêutico
Sirolimo/uso terapêutico
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antirheumatic Agents); 2S9ZZM9Q9V (Bevacizumab); 9Y8NXQ24VQ (Propranolol); W36ZG6FT64 (Sirolimus)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170809
[Lr] Data última revisão:
170809
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170213
[St] Status:MEDLINE


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[PMID]:28104992
[Au] Autor:Kohga A; Kawabe A; Hasegawa Y; Yajima K; Okumura T; Yamashita K; Isogaki J; Suzuki K; Komiyama A
[Ad] Endereço:Atsushi Kohga, Akihiro Kawabe, Yuto Hasegawa, Kiyoshige Yajima, Takuya Okumura, Kimihiro Yamashita, Jun Isogaki, Kenji Suzuki, Division of Surgery, Fujinomiya City General Hospital, Fujinomiya, Shizuoka 4180076, Japan.
[Ti] Título:Ileo-ileal intussusception caused by lymphangioma of the small bowel treated by single-incision laparoscopic-assisted ileal resection.
[So] Source:World J Gastroenterol;23(1):167-172, 2017 Jan 07.
[Is] ISSN:2219-2840
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Intraabdominal lymphangiomas are uncommon; additionally, those affecting the gastrointestinal tract are rare and account for less than 1% of cases. Intussusception caused by a cystic lymphangioma of the small bowel is extremely rare. The patient was a 20-year-old woman who visited our emergency room with a complaint of abdominal pain. A computed tomography image revealed ileo-ileal intussusception with a leading hypovascular mass measuring 1 cm in a diameter. Single-incision laparoscopic-assisted ileal resection was performed. The surgical specimen consisted of a soft polycystic mass. Macroscopically, a pedunculated polyp with a convolutional pattern was found. Microscopically, the inner surfaces of the cysts were covered with a single layer of endothelial cells. On immunohistochemical examination, the endothelial cells were partially positive for D2-40 and CD34. Smooth muscle cells were also found around the cysts. The lesion was diagnosed as a cystic lymphangioma. Dozens of cases of small bowel lymphangiomas have previously been reported. Of these, cases with intussusception were very rare. This is the first case of small bowel intussusception due to lymphangioma treated by single-incision laparoscopic-assisted surgery.
[Mh] Termos MeSH primário: Cistos/complicações
Doenças do Íleo/cirurgia
Neoplasias do Íleo/complicações
Intussuscepção/cirurgia
Laparoscopia/métodos
Linfangioma/complicações
[Mh] Termos MeSH secundário: Dor Abdominal/etiologia
Adulto
Anticorpos Monoclonais Murinos/metabolismo
Antígenos CD34/metabolismo
Cistos/diagnóstico
Cistos/patologia
Cistos/cirurgia
Feminino
Seres Humanos
Doenças do Íleo/diagnóstico
Doenças do Íleo/etiologia
Neoplasias do Íleo/diagnóstico
Neoplasias do Íleo/patologia
Neoplasias do Íleo/cirurgia
Imuno-Histoquímica
Intussuscepção/diagnóstico
Intussuscepção/etiologia
Linfangioma/diagnóstico
Linfangioma/patologia
Linfangioma/cirurgia
Tomografia Computadorizada por Raios X
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antibodies, Monoclonal, Murine-Derived); 0 (Antigens, CD34); 0 (monoclonal antibody D2-40)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170717
[Lr] Data última revisão:
170717
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170121
[St] Status:MEDLINE
[do] DOI:10.3748/wjg.v23.i1.167


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[PMID]:27829197
[Au] Autor:Renacci RM; Bartolotta RJ
[Ad] Endereço:Georgetown University School of Medicine, 3900 Reservoir Road, NW, Washington, DC 20057. Electronic address: rmr92@georgetown.edu.
[Ti] Título:Gorham disease: lymphangiomatosis with massive osteolysis.
[So] Source:Clin Imaging;41:83-85, 2017 Jan - Feb.
[Is] ISSN:1873-4499
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Gorham disease (also referred to as vanishing bone disease or idiopathic massive osteolysis) is a rare skeletal condition that results in the localized replacement of bone with angiomas and fibrosis. The etiology and most effective treatment for this nonhereditary condition remain controversial in the medical literature. To our knowledge, we present the first case of post-traumatic Gorham disease that includes MR imaging (before and after radiation therapy), post-radiation CT with evidence of treatment effect (sclerosis), as well as asymptomatic bilateral renal lymphangiomata.
[Mh] Termos MeSH primário: Nefropatias/complicações
Nefropatias/diagnóstico por imagem
Linfangioma/complicações
Linfangioma/diagnóstico por imagem
Osteólise Essencial/complicações
Osteólise Essencial/diagnóstico por imagem
[Mh] Termos MeSH secundário: Adulto
Seres Humanos
Imagem por Ressonância Magnética
Masculino
Osteólise Essencial/radioterapia
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1701
[Cu] Atualização por classe:170112
[Lr] Data última revisão:
170112
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161110
[St] Status:MEDLINE


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[PMID]:27767681
[Au] Autor:Wright CH; Kusyk D; Rosenberg WS; Sweet JA
[Ad] Endereço:Department of Neurological Surgery, University Hospitals Case Medical Center.
[Ti] Título:Percutaneous transoral clivoplasty and upper cervical vertebroplasties for multifocal skeletal lymphangiomatosis resulting in complete resolution of pain: case report.
[So] Source:J Neurosurg Spine;26(2):171-176, 2017 Feb.
[Is] ISSN:1547-5646
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Lymphangiomatosis is a rare congenital disorder that results in multiorgan system lymphatic invasion. Symptoms due to axial skeletal involvement can range from chronic bone pain to severe deformity resulting in radiculopathy, myelopathy, and even paralysis. The authors present a case of lymphangiomatosis of the clivus, C-1, and C-2, resulting in chronic pain. The patient was successfully treated with percutaneous transoral clivoplasty and vertebroplasty, without disease progression or return of symptoms at 2 years.
[Mh] Termos MeSH primário: Vértebras Cervicais/cirurgia
Fossa Craniana Posterior/cirurgia
Linfangioma/cirurgia
Dor/cirurgia
Neoplasias da Coluna Vertebral/cirurgia
Vertebroplastia/métodos
[Mh] Termos MeSH secundário: Adolescente
Vértebras Cervicais/diagnóstico por imagem
Feminino
Seres Humanos
Linfangioma/diagnóstico por imagem
Linfangioma/fisiopatologia
Dor/diagnóstico por imagem
Dor/fisiopatologia
Neoplasias da Coluna Vertebral/diagnóstico por imagem
Neoplasias da Coluna Vertebral/fisiopatologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1702
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161022
[St] Status:MEDLINE
[do] DOI:10.3171/2016.8.SPINE1675



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