Relevant bibliographies by topics / Angiosarcome – Diagnostic

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Angiosarcome – Diagnostic'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Angiosarcome – Diagnostic"

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Kumar, Parveen. "The Diagnostic Pitfall for Angiosarcoma in one year old child with Extremity Tumor." Journal of Surgical Case Reports and Images 4, no. 1 (2021): 01–03. http://dx.doi.org/10.31579/2690-1897/059.

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Pediatric angiosarcomas are very rare and less studied. There exists a significant degree of confusion in histologically differentiating angiosarcomas from other endothelium derived tumors. We present here a case of right forearm mass in an infant with diagnostic dilemma, which later turned out to be angiosarcoma.
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Perrot, J. L., C. Habougit, A. C. Biron Schneider, et al. "Apport de la microscopie confocale par réflectance in vivo et de l’échographie HD dans le diagnostic d’un angiosarcome du sein." Annales de Dermatologie et de Vénéréologie 146, no. 5 (2019): 410–13. http://dx.doi.org/10.1016/j.annder.2018.12.008.

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Katna, R., A. Deshmukh, E. Sridhar, D. Chaukar, and A. D’Cruz. "Primary angiosarcoma of the larynx: a rare entity." Annals of The Royal College of Surgeons of England 94, no. 4 (2012): e146-e148. http://dx.doi.org/10.1308/003588412x13171221588776.

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Angiosarcomas are extremely rare malignant tumours of the larynx. We present a case of laryngeal angiosarcoma in a 58-yearold man who presented with hoarseness of voice, dysphagia and neck swelling. The patient underwent a total laryngectomy with a pre-operative and frozen section diagnosis of a poorly differentiated carcinoma of the larynx. Histopathological and immunohistochemical evaluation revealed features of a laryngeal angiosarcoma. The case is presented for its rarity and diagnostic difficulty.
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Dowdall, Jayme R., Krisha J. Opfermann, Harold Kim, and Ho-Sheng Lin. "A Case of Radiation-Induced Multifocal Laryngeal Angiosarcoma Presenting as a Diagnostic Dilemma." Case Reports in Otolaryngology 2012 (2012): 1–6. http://dx.doi.org/10.1155/2012/139310.

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Head and neck sarcomas are relatively rare tumors, with angiosarcomas representing a small subset. Angiosarcoma is a malignant endothelial neoplasm characterized by atypical, multilayered, or solid endothelial proliferation with vasoformative architecture. The global incidence of irradiation-associated sarcoma is estimated as between 0.03% and 0.08%. Here we reported the case of an elderly woman previously treated with radiation more than 20 years ago for an unknown primary of head and neck. This interesting case presented as a diagnostic challenge, and multiple biopsies were required to event
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Tabareau-Delalande, Flore, Anne de Muret, Elodie Miquelestorena-Standley, Anne-Valérie Decouvelaere, and Gonzague de Pinieux. "Cutaneous Epithelioid Clear Cells Angiosarcoma in a Young Woman with Congenital Lymphedema." Case Reports in Pathology 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/931973.

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Angiosarcomas are rare aggressive neoplasms that can occur secondary to chronic lymphedema (Stewart-Treves syndrome). Although secondary angiosarcomas are commonly described after-mastectomy and/or after-radiotherapy, few cases have been reported in association with chronic lymphedema of congenital origin. We report the clinical, pathological, and cytogenetic findings in a case of cutaneous epithelioid clear cells angiosarcoma that occurred in a 21-year-old woman with hemibody congenital lymphedema. Surgical biopsies of the tumor mass revealed diffuse epithelioid proliferation of clear atypica
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Vergara Pastrana, Sandra Patricia, Natalia Castañeda Curto, and Carmelo Morales Angulo. "Angiosarcoma Cervical." ACTA DE OTORRINOLARINGOLOGÍA & CIRUGÍA DE CABEZA Y CUELLO 47, no. 1 (2020): 60–63. http://dx.doi.org/10.37076/acorl.v47i1.94.

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Los angiosarcomas son neoplasias de rápido crecimiento originarias en las células endoteliales. Representan un 2% de los sarcomas, y menos del 0.1% de los tumores de cabeza y cuello. Objetivo:Presentar un caso de angiosarcoma cervical en un paciente de la tercera edad. Diseño:Reporte de caso. Materiales y métodos:Mujer de 84 años tratada en el Hospital Universitario Marqués de Valdecilla, con masa asintomática en ángulo mandibular izquierdo de 7-8cms de diámetro. En la TC observamos masa en contacto con parótida izquierda, adenopatías bilaterales. Se realizó PAAF con resultado de angiosarcoma
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Shin, Sandra J., Martin Lesser, and Paul Peter Rosen. "Hemangiomas and Angiosarcomas of the Breast: Diagnostic Utility of Cell Cycle Markers With Emphasis on Ki-67." Archives of Pathology & Laboratory Medicine 131, no. 4 (2007): 538–44. http://dx.doi.org/10.5858/2007-131-538-haaotb.

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Abstract Context.—Vascular tumors comprise a minor subgroup of tumors arising in the breast and represent variants of hemangiomas and angiosarcomas. Diagnostic challenges may arise when differentiating hemangiomas from types I and II angiosarcomas. Ki-67 expression has been used as an adjunct to distinguish between benign and malignant lesions exhibiting histologic overlap at various anatomic sites. Objective.—To investigate the utility of Ki-67 and other cell cycle regulatory proteins (S-phase kinase-associated protein 2 [Skp2], p27, and cyclin D1) in the differential diagnosis of mammary vas
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Morgenstern-Kaplan, Dan, Carlos Manuel Aboitiz-Rivera, Ruben Blachman-Braun, María Eugenia Vázquez-Manríquez, Benito Sarabia-Ortega, and Mario Enrique Baltazares-Lipp. "Primary Cardiac Epithelioid Angiosarcoma in a Latin American Patient: Case Report and Literature Review." Case Reports in Oncological Medicine 2019 (July 30, 2019): 1–4. http://dx.doi.org/10.1155/2019/2641976.

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Cardiac angiosarcoma is a rare and clinically challenging pathology. It is a high-grade primary malignant tumor of the heart tissue that has many variants, of which the epithelioid variant is rarely present in the heart or the great vessels. As with many other cardiac tumors, it is mainly a diagnosis of exclusion and the initial diagnostic test is an echocardiogram followed by a biopsy with immunohistochemistry analysis to ascertain the type of tumor. The differential diagnosis of cardiac tumors is challenging due to the overlapping clinical manifestations with different cardiac tumors and sys
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Rege, Sameer A., Yogesh Takalkar, Amiteshwar Singh, and Archana N. Rijhsinghani. "Primary splenic angiosarcoma: a diagnostic enigma." International Surgery Journal 7, no. 6 (2020): 2065. http://dx.doi.org/10.18203/2349-2902.isj20202438.

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Primary splenic angiosarcomas (PSA) arise from splenic endothelium are rare and impose a diagnostic challenge preoperative. They can present as asymptomatic splenomegaly however; the commonest presentation is abdominal pain. The spleen can rapidly increase in size and can manifest as spontaneous rupture which would cause peritoneal dissemination of disease. Early metastasis of PSA is seen in liver, lungs, lymph nodes and gastrointestinal system. Preoperative diagnosis requires a high index of suspicion and ultrasound, contrast enhanced computerized tomography may essential to differentiate fro
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10

Garcia, Ana Rita, João Ribeiro, Helena Gervásio, and Francisco Castro e. Sousa. "Hepatic Angiosarcoma Masquerading as Hemangioma: A Challenging Differential Diagnosis." Acta Médica Portuguesa 30, no. 10 (2017): 750. http://dx.doi.org/10.20344/amp.8593.

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Hemangiomas are usually diagnosed based on ultrasound findings. The presence of symptoms, rapid growth or atipical imagiological findings should make us consider other diagnoses, including malignant tumors such as angiosarcomas. We describe the case of a previously healthy 46-year-old female without a history of exposure to carcinogens who presented with abdominal pain for two months. Diagnostic work-up revealed elevated gamma-glutamyl transferase and lactate dehydrogenase levels. Abdominal ultrasound described a large nodular lesion in the right lobe of the liver described as a hemangioma. On
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Dissertations / Theses on the topic "Angiosarcome – Diagnostic"

1

Ciroussel, Françoise. "La cancerogenèse par le chlorure de vinyle : modification de l'ADN et dosimétrie moléculaire." Lyon 1, 1990. http://www.theses.fr/1990LYO10057.

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Les effets biologiques du chlorure de vinyle (cvm), cancerogene chez l'homme, sont dependants de son activaton metabolique par les monooxygenases a cytochrome p450. Il en resulte la formation d'un epoxyde reactif: l'oxyde de chlorethylene qui se rearrange rapidement en chloracetaldehyde. Ces metabolites electrophiles peuvent alcoyler les bases des acides nucleiques pour former la n2-etheno-3 guanine la n6-etheno-1 adenine et la n4-etheno-3 cytosine. Des anticorps specifiques diriges contre l'etheno-dado et l'etheno-dcyd ont ete etablis. Ils onot servi de base a la mise au point d'une methode d
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Book chapters on the topic "Angiosarcome – Diagnostic"

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Nielsen, G. Petur, Andrew E. Rosenberg, Vikram Deshpande, Francis J. Hornicek, Susan V. Kattapuram, and Daniel I. Rosenthal. "Angiosarcoma." In Diagnostic Pathology: Bone. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-323-47777-2.50054-9.

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Suster, Saul, and Cesar A. Moran. "Angiosarcoma." In Diagnostic Pathology: Thoracic. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-323-37715-7.50049-9.

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Suster, Saul, and Cesar A. Moran. "Angiosarcoma." In Diagnostic Pathology: Thoracic. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-323-37715-7.50127-4.

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Hicks, David G., and Susan C. Lester. "Angiosarcoma." In Diagnostic Pathology: Breast. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37712-6.50090-9.

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"Angiosarcoma." In Diagnostic Pathology: Cytopathology. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-54763-5.50262-2.

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"Angiosarcoma." In Diagnostic Pathology: Cardiovascular. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-59560-5.50115-6.

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"Angiosarcoma." In Diagnostic Pathology: Neoplastic Dermatopathology. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-323-44310-4.50148-2.

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"Angiosarcoma." In Diagnostic Pathology: Head and Neck. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39255-6.50053-3.

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"Angiosarcoma." In Diagnostic Pathology: Head and Neck. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39255-6.50144-7.

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"Angiosarcoma." In Diagnostic Pathology: Head and Neck. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39255-6.50321-5.

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Conference papers on the topic "Angiosarcome – Diagnostic"

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Taib, NA, CH Yip, WZ W.Mokhtar, et al. "Angiosarcoma of the breast: dilemmas in diagnosis and management." In Asian Breast Diseases Association (ABDA) 3rd Teaching Course: Advances in the Management of Breast Diseases. Asian Breast Diseases Association, 2005. http://dx.doi.org/10.2349/biij.1.1.e6-12.

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Jayender, J., J. Jagannathan, S. Chikarmane, C. P. Raut, and F. A. Jolesz. "Computer-Aided Diagnosis of Breast Angiosarcoma: Results in 14 cases." In Quantitative Medical Imaging. OSA, 2013. http://dx.doi.org/10.1364/qmi.2013.qtu2g.3.

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Choi, Eunju, David Chen, Kim-Anh Lê Cao, Helle Bielefeldt-Ohmann, Caroline A. O'Leary, and Michelle M. Hill. "Abstract 2499: Diagnostic serum biomarkers for canine hemangiosarcoma: a potential model of human angiosarcoma." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-2499.

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4

Subramaniyam, R., and A. Krvavac. "Primary Pulmonary Angiosarcoma with Extension into Left Atrium- Effective Tissue Diagnosis Method." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a6947.

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Journal articles
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