| Excerpt | Reference |
|---|
| "Transition to angiosarcoma is preceded by focal dilatation of sinusoids with even greater activation but dedifferentiation of their lining cells." | ( Popper, H; Thomas, LB, 1975) |
| "Angiosarcomas are tumors with a very malignant biologic behavior and the 5-year survival is very low." | ( Piattelli, A; Tamborrino, F; Tamborrino, G, 1990) |
| "Cutaneous angiosarcoma is an infrequent but aggressive neoplasm involving the skin of the face and scalp." | ( Ariyan, S; Barttelbort, SW; Stahl, R, 1989) |
| "Cutaneous angiosarcoma is a relatively rare but devastating malignant vascular tumor." | ( Liu, MS; Olson, RS; Rounds, DE; Sasaki, GH, 1985) |
| "This type of angiosarcoma is uncommon and carries a poor prognosis: the therapeutic alternatives are discussed." | ( McGibbon, DH; Newton, JA; Spaull, J; Wilson Jones, E, 1985) |
| "Pulmonary artery angiosarcoma is a rare entity." | ( Goldblum, JR; Rice, TW, 1995) |
| "Hepatic angiosarcoma is an infrequent neoplasm representing 1-3% of all the primary liver cancers." | ( Bruguera, M; Castells, A; Forns, X; Navasa, M; Rodés, J; Salgado, M; Sans, M, 1995) |
| "Classic angiosarcoma is an uncommon malignant neoplasm of vascular differentiation which is highly aggressive." | ( Brand, CU; Hunziker, T; von Briel, C; Yawalkar, N, 1996) |
| "Angiosarcomas are an exquisitely infrequent histologic type in this setting and are associated with a universally poor prognosis." | ( Dahut, WL; Lynch, JH; Mordkin, RM, 1997) |
| "Primary renal angiosarcoma is very rare." | ( Anami, M; Chowdhury, PR; Hayashi, T; Horita, Y; Iseki, M; Kanetake, H; Koga, S; Matsuya, F; Saito, Y; Tsuda, N, 1997) |
| "Cutaneous angiosarcoma is a rare aggressive tumour of capillary and lymphatic endothelial cell origin." | ( Natarajan, S; Sinclair, SA; Sviland, L, 1998) |
| "Hemangiomas and hemangiosarcomas are uncommon in rodents and humans and, as such, the mechanisms giving rise to these tumors are poorly understood." | ( Bleavins, MR; de la Iglesia, FA; Dethloff, LA; Duddy, SK; Gorospe, S; Gough, AW; Parker, RF; Rowse, PE, 1999) |
| "Angiosarcoma is an aggressive tumor with a high propensity for both local recurrence and distant metastasis." | ( Antonescu, CR; Kacker, A; Shaha, AR, 1999) |
| "Hemangiosarcomasare uncommon malignant endothelial cell tumors in humans and experimental animal species." | ( Bleavins, MR; de la Iglesia, FA; Duddy, SK; Gorospe, SM, 1999) |
| "Angiosarcomas are rare tumors." | ( Casper, ES; Fata, F; Ilson, D; Kelsen, DP; Leffel, D; O'Reilly, E; Pfister, D; Schwartz, GK, 1999) |
| "Angiosarcoma is an extremely rare bone tumor." | ( Enneking, WF; McDonald, DJ; Sundaram, M, 2002) |
| "Angiosarcoma is a rare and highly malignant vascular neoplasm." | ( Ejima, Y; Hirota, S; Imajo, Y; Kamikonya, N; Kawabe, T; Kishi, K; Matsumoto, A; Murakami, M; Sasaki, R; Soejima, T; Sugimura, K, 2002) |
| "Cardiac angiosarcoma is a rare tumour entity with a poor prognosis." | ( Bockisch, A; Eising, EG; Freudenberg, LS; Lauenstein, T; Rosenbaum, SJ; Schulte-Herbrüggen, J; Wolff, A, 2002) |
| "Angiosarcoma is a malignant tumor of vascular endothelial cells that arises in the head and neck." | ( Baker, LH; Cohen, DS; McGinn, CJ; Morris, JS; Paulino, AF; Pawlik, TM; Rees, R; Sondak, VK, 2003) |
| "Angiosarcoma is a rare vascular tumour accounting for 2% of soft tissue sarcomas, which together represent less than 1% of all cancers." | ( Berman, P; Rich, AL, 2004) |
| "Angiosarcomas are rare, aggressive tumors of vascular origin." | ( Grundmann, T; Lessle, M; Münscher, A, 2004) |
| "Ovarian angiosarcomas are rare tumors which may to be distinguished from other unusual primary ovarian tumors such as clear cell carcinoma, yolk sac tumor and leiomyosarcoma on the basis of histological appearance and immunohistochemistry." | ( Chan, KK; Jha, S; Poole, CJ; Rollason, TP, 2005) |
| "Cutaneous angiosarcoma is a rare aggressive vascular tumor that occurs in elderly patients and is usually located on the head and face." | ( Doi, K; Harada, T; Hirata, C; Ishii, M; Ishina, K; Kamo, R; Nakanishi, T, 2005) |
| "Cutaneous angiosarcomas are rare and constitute less than 1% of all malignant mesenchymal tumours." | ( Bhardwaj, M; Gautam, RK; Kar, HK; Magoon, N; Sharma, A; Sharma, PK, 2005) |
| "Angiosarcoma is an aggressive neoplasm that predominantly affects elderly patients." | ( Khachemoune, A; Lockshin, NA; Selim, A, 2005) |
| "Cutaneous angiosarcoma is a rare and invasive endothelial-derived sarcoma that occurs most frequently in the scalp and facial skin of elderly men." | ( Chen, W; Hsu, WH; Shih, CS; Tseng, GC; Wang, YT, 2006) |
| "Angiosarcomas are rare soft tissue malignancies." | ( Bearz, A; Berretta, M; Berretta, S; Brollo, A; Buonadonna, A; Canzonieri, V; Frustaci, S; Morra, A; Rupolo, M; Tirelli, U, 2006) |
| "Angiosarcoma is a highly malignant neoplasm, which most often develops on the scalp or face of elderly people." | ( Ashizawa, I; Hada, M; Miyashita, Y; Oyama, T; Sakurai, H; Tsukamoto, K, 2006) |
| "Cutaneous angiosarcoma is probably the most malignant neoplasm involving the skin." | ( Cerroni, L; Kaddu, S; Kutzner, H; Menzel, T; Requena, L; Santonja, C; Stutz, N; Weenig, RH, 2007) |
| "Cutaneous angiosarcoma is a rare tumor of endothelial origin, often difficult to diagnose and with an unfavorable prognosis." | ( Bröcker, EB; Goebeler, M; Rose, C; Seitz, CS; Voss, A, 2001) |
| "Angiosarcoma is a rare diagnosis with a poor prognosis." | ( Arndt, CA; Good, AB; Nascimento, A; Welker, KM, 2008) |
| "Cutaneous angiosarcoma is a rare malignant vascular tumor with a poor prognosis, most commonly affecting elderly white men." | ( Douglas, DK; Fonder, MA, 2008) |
| "Cutaneous angiosarcoma is an extremely aggressive tumor." | ( Albertson, D; Bhuller, A; Pan, Z; Sarma, DP; Shehan, JM; Wang, B, 2008) |
| "Cutaneous angiosarcoma is a rare vascular tumor, which is usually located in the head and neck region." | ( Gudewer, E; Hölzle, E; Li, L, 2009) |
| "Aortic angiosarcoma is an exceedingly rare clinical entity." | ( Ellozy, S; Ramjee, V, 2009) |
| "Angiosarcomas are a rare type of malignant vascular tumour characterised by proliferation of tumour cells with vascular endothelial features." | ( Carillo, GA; Carretero, MA; Fontan, EG; Ramos, MB; Rodriguez, AP; Salmon, AS; Tejedor, JL; Vazquez, JE; Ventura, JA, 2010) |
| "Cutaneous angiosarcoma is a very rare but aggressive tumor." | ( Terada, T, 2010) |
| "Epithelioid angiosarcomas are rare aggressive neoplasms that occur most frequently in deep soft tissues." | ( Calonje, E; Fisher, C; Suchak, R; Thway, K; Zelger, B, 2011) |
| "Angiosarcoma is a rare, aggressive soft-tissue sarcoma with a high rate of recurrence and distant metastasis." | ( Carron, MA; Kucuk, O; Lin, HS; Shkoukani, MA; Tulunay, O, 2011) |
| "Angiosarcoma is a highly aggressive soft tissue sarcoma." | ( Arena, MG; Bochicchio, AM; Casali, PG; De Rosa, P; Dei Tos, AP; Morosi, C; Nuzzo, A; Palassini, E; Pilotti, S; Sanfilippo, R; Stacchiotti, S; Turano, S; Vincenzi, B, 2012) |
| "Angiosarcomas are a rare but aggressive form of soft tissue sarcoma." | ( Bay, JO; Bertucci, F; Blay, JY; Bompas, E; Bui, B; Chaigneau, L; Cupissol, D; Delcambre, C; Duffaud, F; Guillemet, C; Isambert, N; Italiano, A; Penel, N; Ray-Coquard, I; Robin, YM, 2012) |
| "Angiosarcoma is a rare neoplasm, accounting for only 1%-2% of all sarcomas." | ( Nakai, R; Tanaka, Y; Tane, S; Tauchi, S; Uchino, K; Yoshimura, M, 2011) |
| "Angiosarcoma is a rare soft-tissue neoplasm occurring most often in the skin and the subcutaneous tissues and very rarely in the gastrointestinal tract." | ( Barnoud, R; Chahbouni, S; Devouassoux-Shisheboran, M; Watkin, E, 2011) |
| "Primary pleural angiosarcoma is a rare and clinically aggressive tumor." | ( Chen, CL; Chow, JM; Chu, JS; Fang, CL; Kao, YC; Wang, KM, 2011) |
| "Hepatic haemangiosarcoma is a deadly malignancy whose aetiology remains poorly understood." | ( Busch, SE; Gurley, KE; Kemp, CJ; Moser, RD, 2012) |
| "Angiosarcomas are malignant endothelial cell tumors with few effective systemic treatments." | ( Buehler, D; Cleary, K; Hafez, GR; Hasenstein, JR; Kasmerchak, K; Kozak, KR; Moody, JS, 2012) |
| "Angiosarcoma is a soft tissue tumour with a dismal prognosis." | ( Deshpande, DJ; Mishra, SN; Nayak, CS, 2012) |
| "Angiosarcoma is an uncommon malignancy, which spread out from the endothelial cells of vessels." | ( Bukawa, H; Fujisawa, Y; Karube, R; Onizawa, K; Otsuka, F; Sasaki, H; Shinozuka, K; Yamagata, K; Yanagawa, T, 2012) |
| "Intimal angiosarcoma is a rare malignant vascular tumor with an aggressive natural history." | ( Choi, SY; Kim, HY; Kim, KI; Min, SK, 2012) |
| "Because cutaneous angiosarcoma is an aggressive tumour with a high propensity for local recurrence and distant metastases, therapy preferably involves a multimodal approach." | ( Iwade, M; Kubo, H; Ohashi, A; Okuyama, R; Shiohara, J; Takata, M; Uhara, H, 2012) |
| "Hemangioma and hemangiosarcoma are extremely rare tumors in the lung of our colony and we believe they are caused by WTC dust." | ( Belpoggi, F; Bua, L; Falcioni, L; Manservigi, M; Soffritti, M; Tibaldi, E, 2013) |
| "Mediastinal angiosarcoma is a rare intrathoracic tumour and the therapeutic approach remains poorly codified." | ( Aubert, M; Coudurier, M; Deroux, A; Destors, M; Girard, N; Lantuejoul, S; Moro-Sibilot, D, 2012) |
| "Angiosarcoma is an uncommon but aggressive tumor of endothelial origin that may occur in the upper extremities of patients with postmastectomy lymphedema (Stewart-Treves syndrome) as well as in other regions." | ( Folpe, AL; Pittelkow, MR; Shon, W; Wada, DA, 2012) |
| "Angiosarcoma is one of the most life-threatening neoplasms with strong resistance to conventional chemotherapy/radiotherapy; consequently, alternative therapeutic agents are urgently required." | ( Abe, R; Aoyagi, S; Fujita, Y; Hata, H; Hoshina, D; Saito, N; Shimizu, H; Yoshioka, N, 2013) |
| "Angiosarcoma is a rare neoplasm of endothelial origin that has limited treatment options and poor five-year survival." | ( Andersen, NJ; Baker, LH; Boguslawski, EA; Dawes, MJ; Duesbery, NS; Dykema, KJ; Froman, RE; Furge, KA; Kamstock, DA; Kitchell, BE; Krivochenitser, RI; Nickoloff, BJ; Thomas, DG, 2013) |
| "Cutaneous angiosarcoma is a life-threatening tumor that is resistant to conventional therapies." | ( Kaneda, Y; Katayama, I; Masuzawa, M; Nakamura, M; Nishizawa, A; Saeki, K; Satoh, T; Takehara, Y; Yokozeki, H, 2013) |
| "Angiosarcomas are rare, aggressive vascular malignancies of endothelial cell differentiation." | ( Grellety, T; Italiano, A, 2013) |
| "Angiosarcoma is a rare malignant neoplasm with a poor prognosis." | ( Hosono, MN; Kamo, R; Miki, Y; Ogino, R; Shimatani, Y; Tada, T; Tamiya, H; Tsutsumi, S, 2013) |
| "Angiosarcomas are rare, aggressive vascular tumours known to express vascular endothelial growth factor (VEGF), a key pro-angiogenic growth factor." | ( Brown, NJ; Reed, MW; Staton, CA; Woll, PJ; Young, RJ, 2014) |
| "Hepatic angiosarcoma is a known consequence of VC exposure, but occupational causality of extra-hepatic angiosarcoma is controversial." | ( Criscuolo, M; Gianicolo, EA; Gianicolo, ME; Portaluri, M; Valerio, J, 2014) |
| "Angiosarcoma is a rare malignant neoplasm of vascular endothelial cells." | ( Aires, D; Blackmon, J; Fraga, G; Gilroy, R; Patel, V; Rajpara, A, 2014) |
| "Primary cardiac angiosarcoma is an extremely rare malignant tumor with various clinical presentations but usually in late stage." | ( Qiu, ZX; Zhang, Q, 2014) |
| "Foamy cell angiosarcoma is probably one of the least common variants of cutaneous angiosarcoma and represents an important diagnostic pitfall." | ( Beneš, T; Benický, M; Fröhlichová, L; Hojstričová, Z; Kazakov, DV; Svajdler, M, 2014) |
| "Cardiac angiosarcomas are a rare form of malignancy." | ( Demir, N; Demirkol, MO; Tokmak, H, 2014) |
| "Angiosarcoma is a rare subtype of soft tissue sarcoma (STS)." | ( Litière, S; Natukunda, A; van der Graaf, WT; Wardelmann, E; Woll, PJ; Young, RJ, 2014) |
| "Angiosarcoma is a malignant tumor of vascular endothelial cell origin." | ( Cazorla, A; Delabrousse, E; Félix, S; Valmary-Degano, S, 2014) |
| "Because paw hemangiosarcomas are easily detectable and scorable for size and growth, this novel mouse model enables accelerated in vivo drug testing for therapies of TSC-related tumors." | ( Auricchio, N; Bronson, RT; Goldman, S; Kwiatkowski, DJ; Lammers, SH; Leech, JD; Sahin, M, 2015) |
| "Angiosarcoma is a rare malignant tumour of endothelial cells." | ( Cosar, R; Ibis, C; Ibis, K; Usta, U, 2015) |
| "Secondary breast angiosarcomas are a well-known entity generally characterized by a poor outcome, especially in patients with advanced disease." | ( Bareggi, C; Blundo, C; Galassi, B; Gambini, D; Locatelli, E; Runza, L; Sosnovskikh, I; Tomirotti, M; Visintin, R, 2015) |
| "Angiosarcomas are most often encountered as sporadic lesions, typically in the scalp or face of elderly patients." | ( Berraies, A; Boudaya, MS; El Mezni, F; Hamzaoui, A; Mlika, M, 2014) |
| "We observed that angiosarcomas are insensitive to mTOR inhibition." | ( Andersen, NJ; Boguslawski, EB; Chambers, CM; Duesbery, NS; Kuk, CY, 2015) |
| "Primary cardiac angiosarcoma is extremely aggressive; however, it is often misdiagnosed because of its rarity." | ( Biasco, G; Brandi, G; Coccolo, F; Gatto, L; Minichillo, S; Nannini, M; Pantaleo, MA, 2015) |
| "Hepatic angiosarcoma is a rare and aggressive vascular neoplasm." | ( Debiec-Rychter, M; Lambrechts, D; Mazzone, M; Prenen, H; Sagaert, X; Sciot, R; Smeets, D, 2015) |
| "Primary splenic angiosarcoma is an extremely rare and aggressive neoplasm." | ( Chang, W; Chen, J; Deng, R; Tao, K; Wu, X; Zhang, P, 2015) |
| "Angiosarcomas are exceedingly rare fatal complications of long-standing metal and Dacron prostheses." | ( Agaimy, A; Ben-Izhak, O; Lorey, T; Rubin, BP; Scharpf, M, 2016) |
| "Angiosarcoma is an aggressive vascular neoplasm with a high propensity for local recurrence." | ( Bonadies, A; Bucher, S; Cabula, C; Campana, LG; Curatolo, P; Grilz, G; Guida, M; Rossi, CR; Rotunno, R; Santoriello, A; Solari, N; Strippoli, S; Valpione, S, 2016) |
| "Angiosarcoma is a malignant neoplastic disease originating from or differentiating toward vascular endothelium, for which systemic pharmacologic treatment has limited durability." | ( Ali, SM; Futreal, A; Miller, VA; Patel, S; Ramesh, N; Ravi, V; Ross, JS; Sanford, EM; Stephens, PJ; Wang, WL, 2016) |
| "Angiosarcomas are rare malignant tumors of vascular origin that represent a genuine therapeutic challenge." | ( André, N; Banavali, SD; Chougule, A; Ghosh, J; Kavallaris, M; MacKenzie, KL; Meurer, M; Pasquier, E; Philip, DSJ; Rekhi, B; Street, J, 2016) |
| "Primary cardiac angiosarcoma is rare and its prognosis very poor." | ( Kaki, N; Kiyama, H; Shimada, N; Shiomi, D, 2016) |
| "Angiosarcomas are rare aggressive neoplasms with a wide variety of anatomic locations, one third of them presenting multifocal." | ( Bader, T; Beck, M; Diebold, J; Egger-Sigg, M; Strobel, K, 2016) |
| "Angiosarcoma is a rare malignant mesenchymal tumor with poor prognosis." | ( Chen, D; Chen, Y; Duan, Y; Kuang, D; Masuzawa, M; Tang, Q; Wan, J; Wang, G; Wang, X; Wang, Y; Yang, Q; Zhang, S; Zhao, X; Zhu, Y, 2016) |
| "Epithelioid angiosarcomas are rare malignant mesenchymal tumors." | ( Galache, CG; Santos-Juanes1, J; Vivanco-Allende, B, 2016) |
| "Angiosarcomas are rare, aggressive malignant mesenchymal tumours with a poor prognosis." | ( Asmar, A; Bülow, J; Cucchi, F; Haarmark, C; Nedergaard, L; Simonsen, L, 2017) |
| "Angiosarcoma is a rare malignant neoplasm derived from endothelial cells, and because advanced angiosarcoma is resistant to standard chemotherapy its prognosis is poor." | ( Abe, R; Amoh, Y; Fukushima, S; Hoshina, D; Ihn, H; Jinnin, M; Kajihara, I; Masuzawa, M; Yamada-Kanazawa, S, 2017) |
| "Angiosarcoma is a rare but aggressive malignancy with a high predilection for the head and neck." | ( Echo, A; Gale, AL; Liberman, SR; Marco, RAW; Zavlin, D, 2017) |
| "Cutaneous angiosarcoma is a rare malignancy that frequently metastasizes the lung." | ( Antaki, J; Jimenez, D; Kamangar, N, 2017) |
| "Epithelioid angiosarcoma is a high grade malignancy sarcoma of soft tissue, which is hard to diagnose and completely excise without causing functional and cosmetic problems." | ( Gao, Y; Liu, J; Lu, YG; Wang, HL; Wang, WS, 2017) |
| "Primary cutaneous angiosarcoma is a rare vascular tumor usually affecting the whole body, and its hypermetabolic features on F-FDG PET/CT may be confused with those of infection, metastasis, or primary malignancy." | ( Hwang, JP, 2017) |
| "Angiosarcomas are rare malignant tumors derived from endothelial cells and occur most commonly in the scalp and the face." | ( Ikeda, M; Kawase, T; Kobari, T; Kobayashi, T; Matsuzuka, T; Murono, S; Nakaegawa, Y; Suzuki, M, 2017) |
| "Primary splenic angiosarcoma is rare." | ( Dong, A; He, T; Wang, Y; Zhao, Q; Zuo, C, 2017) |
| "Human angiosarcoma is a rare malignant vascular tumor associated with extremely poor clinical outcome and generally arising in skin of the head and neck region." | ( Arakawa, H; Chuman, H; Kawai, A; Kinjo, T; Kuyama, K; Masuzawa, M; Miyagi, T; Mori, T; Ohira, A; Takahashi, K; Tsuneki, M; Yamazaki, N; Yoshida, A, 2017) |
| "Angiosarcomas are rare and aggressive soft-tissue sarcomas." | ( Grünhagen, DJ; Hayes, AJ; Huis In 't Veld, EA; Jones, R; Smith, HG; van Akkooi, ACJ; van Coevorden, F; van Houdt, WJ; Verhoef, C, 2017) |
| "Angiosarcomas are highly malignant and rare tumors of vascular or lymphatic endothelial cell origin with a poor prognosis." | ( Andersen, KF; Brittain, JM; Hildebrandt, MG; Hovgaard, D; Nymark, T, 2017) |
| "Primary cardiac angiosarcoma is rare, but it is the most aggressive type of cardiac malignant tumor." | ( Chu, Y; Gao, Y; Li, L; Li, X; Wu, J; Zhang, R, 2017) |
| "Angiosarcoma is a rare aggressive sarcoma that occurs mostly in the skin of the head and neck in the elderly population." | ( Chow, TL; Kwan, CK; Kwan, WW, 2018) |
| "Angiosarcoma is an extremely rare complication of primary lymphoedema; treatment is poorly codified and the prognosis is unfavourable." | ( Dabouz, F; Farhat, MM; Le Guern, A; Modiano, P; Peugniez, C; Quinchon, JF, 2018) |
| "Angiosarcomas are rare, malignant vascular tumors that affect endothelial cells of blood vessels." | ( Ajayi, AA; Clarke, DE; Commins, SV, 2018) |
| "Peritoneal angiosarcoma is an extremely rare sarcoma (0." | ( Chen, WJ; Wu, CC; Wu, IC; Yu, FJ, 2018) |
| "Primary renal angiosarcoma is an exceedingly rare and aggressive neoplasm." | ( Ilyas, G; Inayat, F; Lodhi, HT; Munir, A, 2018) |
| "Breast angiosarcoma is a rare and aggressive tumor." | ( Bozec, L; Cassou-Mounat, T; Champion, L; Huchet, V; Jehanno, N; Laurence, V; Luporsi, M, 2019) |
| "Iliac artery angiosarcoma is rare, and bone metastasis as its presenting initial symptom is extremely rare." | ( Chen, B; Guan, Q; Ji, B; Wang, R; Wang, X, 2019) |
| "Angiosarcoma is a deadly neoplasm of the vascular endothelium." | ( Baig, YC; Cerroni, B; Coronado, R; Decker, WK; DiBernardi, L; Douglass, L; Halpert, MM; Konduri, V; Levitt, JM; Omarbekov, Z; Piscoya, S; Ravi, V; Rodgers, JR; Seelhoff, L; Wilson, N, 2019) |
| "Angiosarcomas are highly aggressive tumors of endothelial origin, which carry a poor prognosis." | ( Alhousseiny, S; Ding, H; Jameel, M; Majeed, Y; Musthak, A; Shaheen, Y; Taha, T; Triggle, CR; Upadhyay, R, 2019) |
| "Hepatic angiosarcoma is an extremely rare diagnosis in children, with fewer than 50 pediatric cases reported in the literature worldwide." | ( Chinnakotla, S; Eidenschink, B; Luquette, M; Neglia, J; Pilbeam, K; Sulciner, M, 2019) |
| "Cardiac angiosarcoma is a rare malignant tumor, for which only surgery has been proven to be effective to date." | ( Davies, H; Jiang, L; Shi, K; Xu, X, 2019) |
| "Primary hepatic angiosarcoma is a rare tumor with poor prognosis." | ( Golob-Schwarzl, N; Haybaeck, J; Hofer, EM; Hoppstädter, J; Kessler, SM; Lackner, C; Leber, B; Liegl-Atzwanger, B; Mischinger, HJ; Schultheiss, CS; Stiegler, P, 2019) |
| "Cutaneous hemangiosarcoma is a malignant neoplasia that frequently occurs in dogs." | ( Azevedo, RB; Dos Santos, JAM; Longo, JPF; Lucci, CM; Muehlmann, LA; Rocha, MST, 2019) |
| "Angiosarcomas are extremely aggressive malignant tumors that arise from vascular endothelial cells." | ( Alqumber, NA; Choi, JW; Kang, MK, 2019) |
| "Angiosarcomas are rare but aggressive tumors with poor prognosis." | ( Chen, C; Fu, D; Guo, H; Li, Y; Liu, M; Liu, Y; Lv, L; Yao, M; Zhang, W; Zhao, L, 2019) |
| "Whilst cutaneous angiosarcoma is rare tumour which primarily affects elderly patients, its management presents a significant therapeutic challenge." | ( Bönisch, N; Langan, EA; Terheyden, P, 2019) |
| "Scalp angiosarcoma is a rare and highly aggressive cutaneous malignancy with poor prognosis and high recurrence rate." | ( Chou, PY; Denadai, R; Huang, CY; Kao, D; Lin, CH, 2019) |
| "Scalp angiosarcoma is a rare and highly aggressive cutaneous malignancy with poor prognosis." | ( Chou, PY; Denadai, R; Huang, CY; Kao, D; Lin, CH, 2019) |
| "Angiosarcomas are malignant neoplasms arising from endothelial cells." | ( Cooper, H; Dorton, D; Farsi, M; Miller, R, 2019) |
| "Angiosarcoma is a rare malignancy concerning around 2% of soft-tissue sarcomas and 5% of cutaneous soft-tissue sarcomas." | ( Barcellini, A; Bonora, M; Brugnatelli, S; Facoetti, A; Fiore, MR; Iannalfi, A; Mirandola, A; Preda, L; Ronchi, S; Secondino, S; Valvo, F; Vischioni, B; Vitolo, V, 2020) |
| "Angiosarcoma is a rare malignant tumor derived from endothelial cells, and its prognosis is poor because advanced angiosarcoma is often resistant to taxane therapy." | ( Abe, R; Amoh, Y; Aoi, J; Fukushima, S; Hoshina, D; Ihn, H; Kajihara, I; Kanemaru, H; Maeda-Otsuka, S; Makino, K; Makino, T; Masuzawa, M; Miyauchi, H; Sakamoto, R; Sawamura, S; Yamada-Kanazawa, S, 2020) |
| "Angiosarcoma is a rare malignant tumor with an aggressive course and poor prognosis." | ( Cataltepe, O; Gessler, D; Lee, V, 2020) |
| "Primary cardiac angiosarcoma is rare and often advances by dissemination." | ( Cheng, J; Ou, X, 2020) |
| "Angiosarcoma is a rare and aggressive malignancy with a high metastatic potential and recurrence rate." | ( Beijnen, JH; Haas, RL; Heinhuis, KM; Huitema, ADR; IJzerman, NS; Koenen, AM; Steeghs, N; van der Graaf, WTA; van Houdt, WJ, 2020) |
| "Cutaneous angiosarcoma is a rare neoplasm." | ( Ariga, T; Heianna, J; Ishikawa, K; Ito, M; Karube, K; Kusada, T; Maemoto, H; Makino, W; Murayama, S; Oota, Y; Shimoji, S; Takehara, S; Zaha, M, 2020) |
| "Angiosarcoma is a highly aggressive mesenchymal tumor." | ( Keam, B; Kim, DW; Kim, M; Kim, SH; Kim, TM; Kim, YJ; Kwak, Y; Moon, KC; Park, C, 2021) |
| "Primary pericardial angiosarcoma is a rare malignant cardiac neoplasm with early metastasis and poor prognosis." | ( Han, L; Li, W; Ye, Z, 2022) |
| "Angiosarcoma is an aggressive malignancy of endothelial cells that carries a high mortality rate." | ( Chanana, P; Dood, R; Haemmerle, M; Holland, EC; Lazar, AJ; Lyons, YA; Mangala, LS; Nagaraja, AS; Ravi, V; Siedel, JH; Sood, AK; Wagner, MJ; Wang, WL, 2021) |
| "Diffuse cutaneous angiosarcomas are rare." | ( Li, L; Xiao, L; Zhang, W, 2021) |
| "Cutaneous angiosarcoma is a type of rare and locally aggressive malignancy requiring individualised treatment owing to paucity of randomised trials." | ( Das, N; Kapoor, R; Khosla, D; Periasamy, K, 2021) |
| "Angiosarcomas are rare but highly aggressive malignancies originating from lymphatic or vascular endothelial cells and may arise from any site in the body." | ( Goyal, S; Kapoor, R; Khosla, D; Madan, R; Periasamy, K; Sali, AP; Singla, V, 2022) |
| "Cutaneous angiosarcoma is a rare and invasive malignant tumor." | ( Bi, S; Cen, Y; Chen, J; Li, J; Yin, X; Zhong, A, 2022) |
| "Cutaneous angiosarcomas is a rare cancer with poor prognoses." | ( Igaki, H; Inaba, K; Itami, J; Kaneda, T; Kashihara, T; Mori, T; Murakami, N; Nakamura, S; Nakayama, H; Nakayama, Y; Namikawa, K; Ogata, D; Okamoto, H; Okuma, K; Takahashi, A; Takahashi, K; Yamakawa, K; Yamazaki, N, 2022) |
| "Angiosarcoma is a rare sarcoma subtype with a poor outcome." | ( Adams, B; Attia, S; Brohl, AS; Burgess, MA; Chawla, S; Cheang, MCU; Cranmer, LD; Ganjoo, KN; Italiano, A; Jones, RL; Liu, L; Maki, RG; Ravi, V; Robertson, L; Theuer, C; Thornton, K, 2022) |
| "Primary hepatic angiosarcoma is a rare but aggressive malignancy." | ( Li, F; Wang, P, 2022) |
| "Angiosarcomas are rare mesenchymal sarcomas that can present as primary cutaneous or noncutaneous disease." | ( Agulnik, M; Kraft, AS; Litwin, S; Movva, S; Ravi, V; Schuetze, SM; Somaiah, N; Tetzlaff, ED; Thiebaud, JA; von Mehren, M, 2022) |
| "Angiosarcoma is a rare cancer that can be found on the skin or in internal organs." | ( Agulnik, M; Kraft, AS; Litwin, S; Movva, S; Ravi, V; Schuetze, SM; Somaiah, N; Tetzlaff, ED; Thiebaud, JA; von Mehren, M, 2022) |
| "Scalp angiosarcoma is a rare and aggressive cancer." | ( Igaki, H; Inaba, K; Kaneda, T; Kashihara, T; Mori, T; Murakami, N; Nakamura, S; Nakayama, H; Nakayama, Y; Namikawa, K; Ogata, D; Okamoto, H; Okuma, K; Takahashi, A; Takahashi, K; Yamazaki, N, 2023) |
| "Scalp angiosarcoma is a rare and aggressive cancer." | ( Igaki, H; Inaba, K; Kaneda, T; Kashihara, T; Mori, T; Murakami, N; Nakamura, S; Nakayama, H; Nakayama, Y; Namikawa, K; Ogata, D; Okamoto, H; Okuma, K; Takahashi, A; Takahashi, K; Yamazaki, N, 2023) |
| "Scalp angiosarcoma is a rare and aggressive cancer." | ( Igaki, H; Inaba, K; Kaneda, T; Kashihara, T; Mori, T; Murakami, N; Nakamura, S; Nakayama, H; Nakayama, Y; Namikawa, K; Ogata, D; Okamoto, H; Okuma, K; Takahashi, A; Takahashi, K; Yamazaki, N, 2023) |
| "Angiosarcoma is a rare, almost universally fatal malignant neoplasm in kidney transplant recipients." | ( Atari, M; Atiemo, K; Friedman, JK; Giusti, S; Jeon, H; Killackey, MT; Paramesh, AS; Vijay, A, 2022) |
| "Angiosarcoma is a rare, almost universally fatal malignant neoplasm in kidney transplant recipients." | ( Atari, M; Atiemo, K; Friedman, JK; Giusti, S; Jeon, H; Killackey, MT; Paramesh, AS; Vijay, A, 2022) |
| "Head and neck skin angiosarcoma is a rare and aggressive tumor (1 % of head and neck tumors)." | ( Guenzi, E; Le Guen, P; Taillé, C; Valery, S, 2023) |
| "Angiosarcomas are a rare subtype representing 1-2% of soft tissue sarcomas." | ( Bay, JO; El-Ghazzi, N, 2023) |
| "Angiosarcoma is a rare, vascular malignancy that arises from endothelial cells of blood vessels." | ( Iqbal, N; Irfan, M; Sharif, A; Vaqar, M, 2023) |
| "Equine haemangiosarcoma is uncommon and only limited reports of successful treatment are available." | ( McGilp, D; Norton, AM; Vasey, JR, 2023) |
| "Primary splenic angiosarcoma is a very rare disease that causes the development of malignant tumors in the vascular endothelium of the splenic sinuses." | ( Zhao, T, 2023) |