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Journal articles on the topic 'Angiosarcome – Diagnostic'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

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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3

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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4

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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6

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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7

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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8

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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9

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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11

Radić, Sonja, Mario Zovak, Anita Galović Marić, Stjepan Baturina, Monica Stephany Kirigin, and Božo Krušlin. "Multiple Primary Angiosarcomas of the Colon." Case Reports in Pathology 2021 (September 9, 2021): 1–5. http://dx.doi.org/10.1155/2021/7237379.

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Introduction. Gastrointestinal angiosarcomas are rare and represent less than 1% of all gastrointestinal tract malignancies, with most occurring in the stomach and small intestine. Occurrence in the colorectal segments is considered extremely rare. Case Report. We describe the case of a 61-year-old male with multiple primary angiosarcomas of the colon who presented with fever and abdominal pain. The patient was initially hospitalized and treated as having an infectious disease. A multislice computed tomography (MSCT) scan revealed multiple soft tissue tumors in the region of the left iliopsoas

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Wong, Alan, and Javier Flores. "Cutaneous angiosarcoma of the head and neck resembling rosacea: A case report." SAGE Open Medical Case Reports 8 (January 2020): 2050313X2094041. http://dx.doi.org/10.1177/2050313x20940419.

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Angiosarcoma is a malignant endothelial cell tumor that involves a variety of anatomic sites with the skin being the most common. Cutaneous angiosarcoma is a diagnostic challenge as it can be confused with lesions such as rosacea, hemangiomas and hematomas. Since the tumor has a propensity for early metastasis and extensive intradermal spread, early diagnostic intervention via punch biopsy may prevent delays in diagnosis and improve tumor resectability and prognosis. We present a case of cutaneous angiosarcoma on the nose and cheeks of a 75-year-old male that resembled rosacea.

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13

Hirani, Fizza, Abigayle Sullivan, Philip Wexler, and Brian Le. "PULMONARY ANGIOSARCOMA: A DIAGNOSTIC CHALLENGE." Chest 158, no. 4 (2020): A1517. http://dx.doi.org/10.1016/j.chest.2020.08.1362.

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14

Zdravkovic, Darko, Miroslav Granic, Marija Zdravkovic, et al. "Breast angiosarcoma one year after adenosquamous endometrial cancer — diagnostic pitfalls." Open Medicine 8, no. 1 (2013): 52–55. http://dx.doi.org/10.2478/s11536-012-0088-7.

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AbstractAngiosarcoma of the breast is a rare and very aggressive tumors originated from endothelial cells lining blood vessels. We report a case of a 55-year-old postmenopausal female with a primary breast angiosarcoma diagnosed just a one year after radical hysterectomy and radiation therapy due to endometrial cancer. The patient initially presented with postmenopausal bleeding. Cytology and biopsy of the endometrium were performed and endometrial adenosquamous carcinoma was diagnosed followed by radical hysterectomy and postoperative local radiatiotherapy (50 Gy). One year later patient pres

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15

Frontario, S. Christopher N., Anna Goldenberg-Sandau, Darshan Roy, and Roy Sandau. "Primary Splenic Angiosarcoma Presenting as Idiopathic Thrombocytopenic Purpura: A Case Report and Review of the Literature." Case Reports in Surgery 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/4173060.

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Angiosarcoma of the spleen is a rare malignancy that arises from vascular endothelial origin. This neoplasm is highly malignant and diagnosis is often delayed due to the vague presentation of clinical symptoms. A case report and concise review of the current diagnostic criteria and surgical treatment are provided to aid in the detection and treatment of this malignancy. We present a case of a 56-year-old female who presented with massive splenomegaly secondary to angiosarcoma of the spleen. The patient suffered from longstanding symptomatic anemia and thrombocytopenia. Diagnosis of a splenic a

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16

Sams, V. G., A. Tsapenko, J. N. Kravitz, and T. E. Gaines. "Angiosarcoma of the Right Atrium Presenting as Syncope and Hemorrhagic Pericardial Tamponade." Case Reports in Surgery 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/829213.

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Angiosarcoma of the heart is a rare malignancy that can present in many ways. It is an important diagnosis to consider in patients presenting with otherwise unexplained tamponade-type symptoms. Here we present a case of a young male who presented with hemorrhagic tamponade and underwent resection of a large angiosarcoma of the right atrium. In this case, we describe the rare presentation of angiosarcoma with its diagnostic approaches, hospital course, clinical management, and discussion.

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17

Gusenbauer, Kaela, Vladimir Ruzhynsky, Ipshita Kak, et al. "Angiosarcoma of the adrenal gland with concurrent contralateral advanced renal cell carcinoma: A diagnostic and management dilemma." Canadian Urological Association Journal 9, no. 5-6 (2015): 302. http://dx.doi.org/10.5489/cuaj.2322.

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Angiosarcoma is a rare high-grade malignant neoplasm with poor clinical outcome and survival rates, occurring most commonly in the skin and soft tissue. It is composed of neoplastic cells that demonstrate endothelial differentiation. The diagnosis of angiosarcoma can be difficult due to its pathohistologic presentation as a poorly differentiated neoplasm with associated secondary changes. We report a case of angiosarcoma of the adrenal gland with concurrent contralateral renal cell carcinoma (RCC) and renal vein thrombus. The presumptive clinical diagnosis was metastatic renal cell carcinoma t

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18

West, John, Shu-Yuan Liao, and Deborah Cho. "Angiosarcoma After Breast Conservation: Diagnostic Pitfalls." Clinical Breast Cancer 8, no. 1 (2008): 94–96. http://dx.doi.org/10.3816/cbc.2008.n.009.

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19

Schmidt de Azevedo, Otavio, Bruna do Nascimento Santos, Nelson de Souza Liboni, Juliano Fernandes da Costa, and Olimpio Daniel de Campos. "Splenic Angiosarcoma: A Diagnostic Splenectomy Finding." Case Reports in Oncology 9, no. 3 (2016): 733–37. http://dx.doi.org/10.1159/000452619.

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Splenic tumors are not frequent. Blood vessel neoplasms are a rare category of tumors and have an extremely low incidence in the spleen. This case report aims to describe a 57-year-old woman in whom a routine imaging examination had shown splenic cysts. During her follow-up, the cysts became larger and increased in number. A diagnostic splenectomy was performed and its analysis showed a rare splenic angiosarcoma.

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20

Shavit, Eran, Afsaneh Alavi, James J. Limacher, and R. Gary Sibbald. "Angiosarcoma complicating lower leg elephantiasis in a male patient: An unusual clinical complication, case report and literature review." SAGE Open Medical Case Reports 6 (January 2018): 2050313X1879634. http://dx.doi.org/10.1177/2050313x18796343.

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Chronic lymphedema is rarely complicated by an angiosarcoma. Angiosarcoma superimposed on chronic lymphedema (Stewart–Treves syndrome) is usually seen post breast cancer surgery accompanied by lymph node resection of the axilla. This is a case report of a 59-year-old male patient with elephantiasis that developed an angiosarcoma of the lower leg. He died a month after the diagnostic biopsy was obtained. This is a rare multifocal tumor in a male with an unusual lower leg location. We reviewed the literature and the need to differentiate this often deadly lesion from a Kaposi’s sarcoma.

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21

Akkaya, Zehra, Aysegul Gursoy, and Ayse Erden. "The disastrous “sun ray” sign in cardiac magnetic resonance: an indicator of angiosarcoma." Cardiology in the Young 24, no. 5 (2013): 929–31. http://dx.doi.org/10.1017/s1047951113001455.

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AbstractDistinguishing the benign and malignant cardiac masses is usually a diagnostic challenge, and safe, non-invasive, and reliable techniques are necessary to avoid any delay in treatment. The previously described “sun ray” appearance is an important sign in the diagnosis of cardiac angiosarcoma, and in this report we present 3-T magnetic resonance imaging findings to distinguish the rare but fatal cardiac angiosarcoma.

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22

Zincone, Gian Emilio, Paolo Perego, Gian Marco Rossi, and Giorgio Bovo. "A Case of Breast Angiosarcoma: Diagnostic Imaging and Review of the Literature." Tumori Journal 81, no. 5 (1995): 387–90. http://dx.doi.org/10.1177/030089169508100517.

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Primary angiosarcoma of the breast is a rare tumor, with approximately 170 cases reported in the literature (1-3, 10, 11, 15). Reports on the imaging characteristics of these tumors have been occasional until a recent review by Liberman et al. (11). Diagnostic imaging of the masses include mammographic and ultrasound examinations (5): the imaging characteristics of the tumor can be nonspecific and sometimes heterogeneous (11). Only recently was one case evaluated with magnetic resonance imaging (11). We present the mammographic and sonographic features of a case of primary angiosarcoma of the

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Qayyum, Sohail, Jignesh G. Parikh, and Nadeem Zafar. "Primary Renal Angiosarcoma with Extensive Necrosis: A Difficult Diagnosis." Case Reports in Pathology 2014 (2014): 1–3. http://dx.doi.org/10.1155/2014/416170.

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Angiosarcoma of the kidney is an exceedingly rare and aggressive neoplasm. Very few cases have been reported in the English literature to date. We report a case of primary renal angiosarcoma with extensive necrosis and discuss its diagnostic difficulties. An 86-year-old male presented with a 12 cm necrotic renal mass and multiple pulmonary and hepatic nodules. A CT guided renal biopsy revealed extensive necrosis and few vascular channels lined by malignant endothelial cells. Diagnosis was given on a morphologic base and proven by an immunohistochemical study. Primary renal angiosarcoma should

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Ostańska, Elżbieta, David Aebisher, Ewa Kaznowska, and Dorota Bartusik-Aebisher. "Primary breast angiosarcoma – a case report." European Journal of Clinical and Experimental Medicine 18, no. 4 (2021): 331–34. http://dx.doi.org/10.15584/ejcem.2020.4.12.

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Introduction. Angiosarcoma is a rare breast cancer that can be primary or secondary after surgery or after breast cancer radiotherapy. It is important that breast angiosarcoma belongs to tumors with a non-specific clinical and radiological picture. Aim. The study of the biopsies contained aggressive vasomotor hyperplasia. Description of the case. The presented case concerns the primary angiosarcoma of the right breast in a 56-year-old woman who had never had a surgical procedure before, nor radiotherapy in the area of the breast. Conclusion. Histopathological examination supported by immunohis

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Hart, Jesse, and Srinivas Mandavilli. "Epithelioid Angiosarcoma: A Brief Diagnostic Review and Differential Diagnosis." Archives of Pathology & Laboratory Medicine 135, no. 2 (2011): 268–72. http://dx.doi.org/10.5858/135.2.268.

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Abstract Epithelioid angiosarcoma is a highly aggressive endothelial cell malignancy, most commonly arising in the deep soft tissues, but a variety of primary sites, including the adrenals, thyroid, skin, and bone, are encountered. On hematoxylin-eosin–stained sections, the pathologist encounters sheets of large, mildly to moderately pleomorphic epithelioid cells, with abundant eosinophilic cytoplasm, vesicular nuclei, and prominent nucleoli. Obvious vasoformative foci may not be present, creating confusion with metastatic carcinomas, malignant mesothelioma, melanoma, anaplastic lymphoma, epit

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Siderits, Richard, Frederick Poblete, Biren Saraiya, Cheryl Rimmer, Anup Hazra, and Le Aye. "Angiosarcoma of Small Bowel Presenting with Obstruction: Novel Observations on a Rare Diagnostic Entity with Unique Clinical Presentation." Case Reports in Gastrointestinal Medicine 2012 (2012): 1–5. http://dx.doi.org/10.1155/2012/480135.

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We present a case of angiosarcoma in small bowel, presenting with partial small bowel obstruction in a 79-year-old man with no history of radiation, chemotherapy, toxin exposure, or previous operative intervention. Angiosarcoma of small bowel is a rare entity which may present with nausea, abdominal pain, recurrent bleeding, and usually a history of prior radiation or exposure to specific toxins (polyvinyl chloride). Angiosarcoma of small bowel tends to spread rapidly and has a poor prognosis. We review the surgical and oncologic challenges. We report unique macroscopic findings of raised hype

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27

Rodríguez Israel, Melissa, Andrés Garzona Navas, Ana Beatriz Argüelles Argüello, and Ruy Vargas Baldares. "Disnea de causa insospechada." Revista de ecocardiografía práctica y otras técnicas de imagen cardíaca 3, no. 2 (2020): 18–21. http://dx.doi.org/10.37615/retic.v3n2a6.

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El angiosarcoma primario de pericardio es una patología extremadamente infrecuente, con muy mal pronóstico. Se presenta un paciente ingresado por un cuadro constitucional y disnea en el que se diagnostica un derrame pericárdico hemorrágico asociado a un tumor maligno de pericardio, y que termina falleciendo. La autopsia confirmó el diagnóstico de angiosarcoma de pericardio.

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Abegunde, Ayokunle T., Efe Aisien, Benjamin Mba, Rohini Chennuri, and Marin Sekosan. "Fulminant Hepatic Failure Secondary to Primary Hepatic Angiosarcoma." Case Reports in Gastrointestinal Medicine 2015 (2015): 1–8. http://dx.doi.org/10.1155/2015/869746.

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Background. Hepatic angiosarcoma is a rare and aggressive tumor that often presents at an advanced stage with nonspecific symptoms.Objective. To report a case of primary hepatic angiosarcoma in an otherwise healthy man with normal liver function tests two months prior to presenting with a short period of jaundice that progressed to fulminant hepatic failure.Methods. Case report and review of literature.Conclusion. This case illustrates the rapidity of progression to death after the onset of symptoms in a patient with hepatic angiosarcoma. Research on early diagnostic strategies and newer thera

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Delacruz, Victor, Merce Jorda, Carmen Gomez-Fernandez, Pasquale Benedetto, and Parvin Ganjei. "Fine-Needle Aspiration Diagnosis of Angiosarcoma of the Spleen: A Case Report and Review of the Literature." Archives of Pathology & Laboratory Medicine 129, no. 8 (2005): 1054–56. http://dx.doi.org/10.5858/2005-129-1054-fadoao.

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Abstract Primary angiosarcoma of the spleen is a very rare neoplasm with a poor prognosis. The definitive diagnosis is usually based on the histologic evaluation of the splenectomy specimen. We describe a case of angiosarcoma diagnosed by fine-needle aspiration cytology prior to splenectomy. A 69-year-old white woman presented with heterogeneous lesions in the spleen during a follow-up computed tomographic scan for a history of liposarcoma of the right buttock. A malignant endothelial neoplasm was diagnosed by fine-needle aspiration cytology using immunocytochemistry, and a splenectomy confirm

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30

Shchava, S. N., E. A. Serdyukova, N. A. Redkina, E. I. Faybisovich, and R. A. Mansurov. "Clinical case of angiosarcoma: differential diagnostic pathway." Klinicheskaya dermatologiya i venerologiya 18, no. 6 (2019): 699. http://dx.doi.org/10.17116/klinderma201918061699.

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Matsumura, Soichi, Takahiro Yoshida, Ayumu Taniguchi, Takahiro Imanaka, Kazuaki Yamanaka, and Hidefumi Kishikawa. "Primary perirenal angiosarcoma: A preoperative diagnostic challenge." Urology Case Reports 32 (September 2020): 101228. http://dx.doi.org/10.1016/j.eucr.2020.101228.

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32

Krishnan, Tharani, Gosta Pettersson, Rahul Mukherjee, and Nimit Singhal. "Cardiac angiosarcoma: A diagnostic and therapeutic challenge." Journal of Cardiology Cases 22, no. 2 (2020): 90–93. http://dx.doi.org/10.1016/j.jccase.2020.04.010.

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Anthonissen, N., T. Menting, M. Verkroost, and W. Morshuis. "Angiosarcoma of the Descending Aorta, Diagnostic Difficulties." EJVES Short Reports 32 (2016): 4–6. http://dx.doi.org/10.1016/j.ejvssr.2016.04.002.

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Tanking, Chonthicha, and Supawat Ratanapo. "Diagnostic challenge in primary cardiac lymphoma: a case report." European Heart Journal - Case Reports 4, no. 5 (2020): 1–5. http://dx.doi.org/10.1093/ehjcr/ytaa160.

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Abstract Background Primary cardiac lymphoma is an extra-nodal non-Hodgkin’s lymphoma, which usually responds well to chemotherapy. The disease has high mortality rate unless it is recognized and treated in time. Tissue pathology is crucially the diagnosis gold standard for treatment plan. This is a case report of an elderly female who presented with a huge right-sided cardiac tumour obstructing tricuspid flow. Case summary An 81-year-old Asian female presented with clinical right-sided heart failure. Echocardiogram showed a large mass compressing and obliterating the right atrium. Trans-jugul

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35

Pisani, Paolo, Marco Krengli, Antonio Ramponi, Massimo Olina, and Francesco Pia. "Angiosarcoma of the hypopharynx." Journal of Laryngology & Otology 108, no. 10 (1994): 905–8. http://dx.doi.org/10.1017/s0022215100128476.

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AbstractAngiosarcoma is a tumour of endothelial origin rarely found in the head and neck. A case of angiosarcoma of the pyriform sinus, treated by surgery and post-operative radiotherapy, is reported, providing a cue for discussion of the diagnostic, clinical and pathological pecularities of the tumour in the light of personal experience and the published data.

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Sadhu, Sagar, Sanjib Pattari, Forqan Shaikh, Rakesh Verma, and Manas Kr Roy. "Colonic metastasis from subcutaneous angiosarcoma: A diagnostic dilemma." Indian Journal of Surgery 72, S1 (2010): 328–30. http://dx.doi.org/10.1007/s12262-010-0089-1.

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37

Keenan, Niall, Simon Davies, Mary N. Sheppard, Alicia Maceira, Walter Serino, and Raad H. Mohiaddin. "Angiosarcoma of the right atrium: A diagnostic dilemma." International Journal of Cardiology 113, no. 3 (2006): 425–26. http://dx.doi.org/10.1016/j.ijcard.2005.07.083.

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Jovanovic, Luka, Predrag Filipovic, Jelena Dedovic-Stojakovic, et al. "The role of c-MYC expression in the diagnostic and clinical confirmation of radiation-induced angiosarcoma: A case report and a review of literature." Vojnosanitetski pregled, no. 00 (2021): 28. http://dx.doi.org/10.2298/vsp201207028j.

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Introduction. Angiosarcomas (AS) arising from vascular tissue, accounting for 3.3% of all sarcomas, have a poor prognosis. Radiation-induced AS is a rare late complication of radiotherapy treatment and is characterized by a gene expression profile such as amplification of the MYC oncogene, by which we can distinguish primary from the secondary induced tumor. Case report, At 77-year-old patient, with early-stage endometrial adenocarcinoma, the radical hysterectomy with bilateral salpingo-oophorectomy was initially done. According to pathological risk factors, the postoperative external beam con

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Tenjarla, Sharang, Lucy Ashley Sheils, Theresa M. Kwiatkowski, and Sheema Chawla. "Cutaneous Angiosarcoma of the Foot: A Case Report and Review of the Literature." Case Reports in Oncological Medicine 2014 (2014): 1–5. http://dx.doi.org/10.1155/2014/657876.

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Primary Angiosarcoma of the skin of the foot is very rare. Angiosarcoma is typically treated with resection and wide-field postoperative radiation therapy. Chemotherapy and radiation therapy have also been used. Regardless of the treatment, the risk of local and distant relapse remains high for this disease. We present a case of an elderly patient who developed cutaneous angiosarcoma of the foot. It posed as a diagnostic dilemma at presentation. Chronic lymphedema was a possible predisposing factor. Given his age, preexisting renal dysfunction, refusal of surgery, and preference not to receive

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Peterson, Cheryl Brus, and Solange Beauregard. "Radiation-Induced Breast Angiosarcoma." Journal of Cutaneous Medicine and Surgery 20, no. 4 (2016): 304–7. http://dx.doi.org/10.1177/1203475416631525.

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Importance: Radiation-induced angiosarcoma after conservative treatment of breast cancer affects a small percentage of patients but has a significant impact on survival. Early detection requires a high index of suspicion and is important for optimal management of this aggressive disease. Observations: The patient reported here presented with radiation-induced angiosarcoma of the left breast 14 years after radiation therapy. Histopathology was positive for anti-CD31, anti-CD34, D2-40, and anti–factor VIII (von Willebrand). She underwent a total mastectomy and is still in remission 20 months lat

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Anandan, Jaimie, Apuca Susan Mathew, Preethi T. Ramadas, Rakhi M. R., and Felicia Prema R. "Aggressive epithelioid angiosarcoma of the scalp: a diagnostic challenge." International Journal of Biomedical Research 6, no. 8 (2015): 588. http://dx.doi.org/10.7439/ijbr.v6i8.2343.

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Abdin-Mohamed, M., J. Ledingham, F. Witham, and F. McCrae. "Aortic angiosarcoma mimicking large-vessel vasculitis: a diagnostic dilemma." Rheumatology 47, no. 5 (2008): 645. http://dx.doi.org/10.1093/rheumatology/ken115.

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Kiyozuka, Yasuhiko, Hiroshi Koyama, Masashi Nakata, et al. "Diagnostic Cytopathology in Type II Angiosarcoma of the Breast." Acta Cytologica 49, no. 5 (2005): 560–66. http://dx.doi.org/10.1159/000326206.

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Ng, W. K., R. J. Collins, D. Law, and E. Gwi. "Cutaneous epithelioid angiosarcoma: A potential diagnostic trap for cytopathologists." Diagnostic Cytopathology 16, no. 2 (1997): 160–67. http://dx.doi.org/10.1002/(sici)1097-0339(199702)16:2<160::aid-dc14>3.0.co;2-k.

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Balaji G, Gopisankar, Justin S. V. Arockiaraj, Alfred Cyril Roy, and Burad Deepak. "Primary Epithelioid Angiosarcoma of the Calcaneum: A Diagnostic Dilemma." Journal of Foot and Ankle Surgery 53, no. 2 (2014): 239–42. http://dx.doi.org/10.1053/j.jfas.2013.10.010.

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Wang, Hanping, Juhong Shi, Hongrui Liu, et al. "Clinical and diagnostic features of angiosarcoma with pulmonary metastases." Medicine 96, no. 36 (2017): e8033. http://dx.doi.org/10.1097/md.0000000000008033.

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Gayathri, J., Hosapatna L. Kishanprasad, Bhat Shubha, Shetty K. Jayaprakash, and K. R. Bhagwan. "A Rare Case of Epithelioid Angiosarcoma Exhibiting Diagnostic Ambiguity." Indian Journal of Surgical Oncology 8, no. 3 (2017): 447–50. http://dx.doi.org/10.1007/s13193-017-0669-7.

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Schlachtenberger, Georg, Stephen Gerfer, Axel Kröner, and Thorsten Wahlers. "Angiosarcoma of the Left Atrium: A Case Report." Thoracic and Cardiovascular Surgeon Reports 07, no. 01 (2018): e4-e6. http://dx.doi.org/10.1055/s-0038-1627443.

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Background Primary cardiac tumors are rare, and many diagnosed tumors are benign with an incidence of 0.001% to 0.03%. The primary angiosarcoma is one of the malignant entities. Discussion We discuss a case report of a 76-year-old male who underwent a preoperative diagnosis for an upcoming shoulder operation when his cardiologist diagnosed a large cardiac tumor. The patient was referred to our department where he received further diagnostics. The transesophageal echocardiography and the cardiac-magnetic resonance imaging showed a massive tumor with a dimension of 8.6 × 5.6 cm with no signs of

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Mikami, Tetuo, Makoto Saegusa, Fumiyuki Akino, et al. "A Kaposi-like Variant of Splenic Angiosarcoma Lacking Association With Human Herpesvirus 8." Archives of Pathology & Laboratory Medicine 126, no. 2 (2002): 191–94. http://dx.doi.org/10.5858/2002-126-0191-aklvos.

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Abstract We report the case of a Kaposi-like variant of splenic angiosarcoma in a 28-year-old woman. The tumor featured a Kaposi sarcoma–like spindle cell proliferation with slit formation and markedly dilated spongelike vascular channels filled with erythrocytes. Thirteen months following the initial splenectomy, metastatic lesions were found in the patient's liver and bone marrow. The proliferating cells were positive for factor VIII–associated antigen and CD34. The human herpesvirus 8 genome, which is regarded as a diagnostic feature of Kaposi sarcoma, was not detected by polymerase chain r

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Shilpa, Kanathur, B. Leelavathy, Divya Gorur, and Dayanand Biligi. "Early-onset epithelioid angiosarcoma: Diagnostic enigma, a rare case report." Indian Journal of Dermatopathology and Diagnostic Dermatology 6, no. 1 (2019): 36. http://dx.doi.org/10.4103/ijdpdd.ijdpdd_58_18.

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