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Items 1 to 27 of about 27
1. Elli M, Can B, Ceyhan M, Pinarli FG, Dagdemir A, Ayyildiz HS, Gürsel B, Dagçinar A: Intrathoracic malignant peripheral nerve sheath tumor with angiosarcoma in a child with NF1. Tumori; 2007 Nov-Dec;93(6):641-4
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  • [Title] Intrathoracic malignant peripheral nerve sheath tumor with angiosarcoma in a child with NF1.
  • We report on a 13-year-old boy with intrathoracic angiosarcoma arising in MPNST associated with NF1.
  • [MeSH-major] Hemangiosarcoma. Neoplasms, Multiple Primary. Nerve Sheath Neoplasms. Neurofibromatosis 1

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  • (PMID = 18338507.001).
  • [ISSN] 0300-8916
  • [Journal-full-title] Tumori
  • [ISO-abbreviation] Tumori
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
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2. Mejía AF, Gierbolini L, Jacob B, Westmoreland SV: Pediatric hepatic hemangiosarcoma in a rhesus macaque (Macaca mulatta). J Med Primatol; 2009 Apr;38(2):121-4
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  • [Title] Pediatric hepatic hemangiosarcoma in a rhesus macaque (Macaca mulatta).
  • BACKGROUND: Pediatric hepatic angiosarcoma is a rare condition in children with poor prognosis.
  • Hemangiosarcoma in non-human primates is a rare finding.
  • Immunohistochemistry was used to characterize the hepatic hemangiosarcoma.
  • Histopathology confirmed a poorly differentiated hemangiosarcoma.
  • CONCLUSIONS: Hemangiosarcoma in non-human primates has been rarely reported.
  • Due to the young age of this monkey and the particular solid pattern throughout the mass this neoplasm resembles pediatric hepatic angiosarcoma in humans.

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  • [Cites] J Med Primatol. 2001 Apr;30(2):127-30 [11491406.001]
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  • [Cites] Pediatr Radiol. 2001 Aug;31(8):533-45 [11550763.001]
  • (PMID = 18671765.001).
  • [ISSN] 1600-0684
  • [Journal-full-title] Journal of medical primatology
  • [ISO-abbreviation] J. Med. Primatol.
  • [Language] ENG
  • [Grant] United States / NCRR NIH HHS / RR / T32 RR007000; United States / NCRR NIH HHS / RR / U42 RR016021; United States / NCRR NIH HHS / RR / P51 RR000168; United States / NCRR NIH HHS / RR / P40 RR003640; United States / NCRR NIH HHS / RR / 2 P40RR003640; United States / NCRR NIH HHS / RR / T32 RR007000-32; United States / NCRR NIH HHS / RR / RR007000-32
  • [Publication-type] Case Reports; Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] Denmark
  • [Other-IDs] NLM/ NIHMS93255; NLM/ PMC2664403
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3. Hertl M, Cosimi AB: Liver transplantation for malignancy. Oncologist; 2005 Apr;10(4):269-81
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  • There is no controversy that hepatoblastoma is an excellent indication in pediatric patients with unresectable tumors.
  • Epitheloid hemangioendothelioma is also an appropriate indication for liver transplantation, unlike angiosarcoma.

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  • (PMID = 15821247.001).
  • [ISSN] 1083-7159
  • [Journal-full-title] The oncologist
  • [ISO-abbreviation] Oncologist
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 62
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4. Good AB, Nascimento A, Welker KM, Arndt CA: Congenital angiosarcoma with transient response to paclitaxel. J Pediatr Hematol Oncol; 2008 Jun;30(6):451-3
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  • [Title] Congenital angiosarcoma with transient response to paclitaxel.
  • Angiosarcoma is a rare diagnosis with a poor prognosis.
  • We report the first known case of congenital angiosarcoma.
  • We also report a transient response with paclitaxel, an agent that may have a role in unresectable angiosarcoma.
  • [MeSH-major] Antineoplastic Agents, Phytogenic / therapeutic use. Head and Neck Neoplasms / congenital. Head and Neck Neoplasms / drug therapy. Hemangiosarcoma / congenital. Hemangiosarcoma / drug therapy. Paclitaxel / therapeutic use

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  • (PMID = 18525462.001).
  • [ISSN] 1077-4114
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Phytogenic; P88XT4IS4D / Paclitaxel
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5. Hsu JT, Ueng SH, Hwang TL, Chen HM, Jan YY, Chen MF: Primary angiosarcoma of the spleen in a child with long-term survival. Pediatr Surg Int; 2007 Aug;23(8):807-10

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  • [Title] Primary angiosarcoma of the spleen in a child with long-term survival.
  • Primary angiosarcoma of the spleen is a very rare and aggressive neoplasm with poor prognosis.
  • Splenic angiosarcoma rarely occurs in the pediatric group (18 years or younger).
  • Survival duration for pediatric patients is very limited.
  • We report a 7-year-old boy with splenic angiosarcoma presented with left upper quadrant abdominal pain and a palpable abdominal mass.
  • Histological examination of the surgical specimen showed that this tumor had typical feature of angiosarcoma including vasoformative architecture, highly pleomorphic tumor cells with irregular, hyperchromatic and prominent nucleoli, and some mitosis.
  • This is the longest reported duration of survival in a patient with splenic angiosarcoma.
  • [MeSH-major] Hemangiosarcoma. Splenic Neoplasms

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  • (PMID = 17641924.001).
  • [ISSN] 0179-0358
  • [Journal-full-title] Pediatric surgery international
  • [ISO-abbreviation] Pediatr. Surg. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
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6. Hsu JT, Chen HM, Lin CY, Yeh CN, Hwang TL, Jan YY, Chen MF: Primary angiosarcoma of the spleen. J Surg Oncol; 2005 Dec 15;92(4):312-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary angiosarcoma of the spleen.
  • BACKGROUND AND OBJECTIVES: Primary splenic angiosarcoma is a very rare and aggressive neoplasm with a high metastatic rate and dismal prognosis.
  • METHODS: The records of all cases of primary splenic angiosarcoma treated at Chang Gung Memorial Hospital from April 1991 to July 2004 were retrospectively reviewed.
  • CONCLUSIONS: The clinical presentations of splenic angiosarcoma were similar to those of previous reports apart from the higher rate of splenomegaly observed in this study.
  • In contrast to reported pediatric cases, our patient achieved long-term disease-free survival after splenectomy alone.
  • [MeSH-major] Hemangiosarcoma. Splenic Neoplasms

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  • [Copyright] 2005 Wiley-Liss, Inc.
  • (PMID = 16299797.001).
  • [ISSN] 0022-4790
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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7. Ayadi L, Khabir A: Pediatric angiosarcoma of soft tissue: a rare clinicopathologic entity. Arch Pathol Lab Med; 2010 Mar;134(3):481-5
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  • [Title] Pediatric angiosarcoma of soft tissue: a rare clinicopathologic entity.
  • Childhood angiosarcomas are exceedingly rare.
  • The differential diagnosis includes Kaposi sarcoma, epithelioid hemangioendothelioma, hemangiopericytoma, and spindle cell hemangioendothelioma whose prognosis is different.
  • [MeSH-major] Head and Neck Neoplasms / pathology. Hemangiosarcoma / pathology. Mediastinal Neoplasms / pathology. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adolescent. Biomarkers, Tumor / analysis. Child. Child, Preschool. Combined Modality Therapy. Diagnosis, Differential. Female. Hemangioendothelioma, Epithelioid / diagnosis. Hemangiopericytoma / diagnosis. Humans. Infant. Male. Prognosis. Sarcoma, Kaposi / diagnosis

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  • (PMID = 20196675.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  • [Number-of-references] 17
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8. Nord KM, Kandel J, Lefkowitch JH, Lobritto SJ, Morel KD, North PE, Garzon MC: Multiple cutaneous infantile hemangiomas associated with hepatic angiosarcoma: case report and review of the literature. Pediatrics; 2006 Sep;118(3):e907-13
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  • [Title] Multiple cutaneous infantile hemangiomas associated with hepatic angiosarcoma: case report and review of the literature.
  • Histopathologic evaluation of the liver revealed a diagnosis of type 2 infantile hepatic hemangioendothelioma (regarded as synonymous with angiosarcoma) rather than benign infantile hemangioma of the liver.
  • Subsequent skin biopsies confirmed that her multiple cutaneous lesions were infantile hemangiomas and not metastatic angiosarcoma.
  • We report this case and a review of the literature on pediatric angiosarcoma of the liver associated with cutaneous infantile hemangiomas.
  • [MeSH-major] Hemangioma / pathology. Hemangiosarcoma / pathology. Liver Neoplasms / pathology. Skin Neoplasms / pathology

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  • [ErratumIn] Pediatrics. 2007 Jun;119(6):1271
  • (PMID = 16880251.001).
  • [ISSN] 1098-4275
  • [Journal-full-title] Pediatrics
  • [ISO-abbreviation] Pediatrics
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 27
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9. Lach B, Hassounah M, Khafaga Y: Primary angiosarcoma of the brain in a child. Fetal Pediatr Pathol; 2008;27(3):175-83
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  • [Title] Primary angiosarcoma of the brain in a child.
  • We describe a pediatric case of primary angiosarcoma of the brain displaying striking intravascular papillary pattern, consistent with the "Dabska tumor," often in continuity with a massive, multifocal intravascular papillary endothelial hyperplasia.
  • Colocalization of these lesions suggests the development of a papillary angiosarcoma in the pre-existing vascular malformation.
  • [MeSH-major] Brain Neoplasms. Hemangiosarcoma. Neoplasms, Vascular Tissue

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  • (PMID = 18633770.001).
  • [ISSN] 1551-3823
  • [Journal-full-title] Fetal and pediatric pathology
  • [ISO-abbreviation] Fetal Pediatr Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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10. Syed SP, Martin AM, Haupt HM, Arenas-Elliot CP, Brooks JJ: Angiostatin receptor annexin II in vascular tumors including angiosarcoma. Hum Pathol; 2007 Mar;38(3):508-13
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  • [Title] Angiostatin receptor annexin II in vascular tumors including angiosarcoma.
  • Thirty-eight (38) vascular tumors tested included: hemangiomas - capillary [4], cavernous [6], lobular capillary [6], intramuscular hemangioma [3], spindle cell [1], and epithelioid hemangioma [4]; epithelioid hemangioendothelioma [3]; angiosarcoma [7], 4 of which were epithelioid; and angiolipomas [4].
  • To our knowledge this is the first demonstration of an angiostatin receptor (ANX2) in vascular endothelial tumors including angiosarcoma.
  • ANX2 reactivity may be the basis of treatment for a variety of benign tumors, especially in pediatric patients, and may offer a new and potentially less toxic therapy for angiosarcoma.
  • [MeSH-major] Annexin A2 / metabolism. Hemangioma / metabolism. Hemangiosarcoma / metabolism. Neoplasms, Vascular Tissue / metabolism

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  • (PMID = 17239928.001).
  • [ISSN] 0046-8177
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Annexin A2
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11. Renukaswamy GM, Boardman SJ, Sebire NJ, Hartley BE: Angiosarcoma of skull base in a 1-year-old child--a case report. Int J Pediatr Otorhinolaryngol; 2009 Nov;73(11):1598-600
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  • [Title] Angiosarcoma of skull base in a 1-year-old child--a case report.
  • Angiosarcoma is a rare tumour of endothelial cell origin whilst malignant skull base tumours are highly unusual in paediatric patients.
  • This case reports an angiosarcoma involving the clivus and basi-sphenoid region of the skull base, in a 1-year-old boy.
  • This tumour is extremely rare in childhood, particularly in this site.
  • The histological features were consistent with a high-grade haemangioendothelioma, categorised as an angiosarcoma.
  • This is the youngest reported patient, to our knowledge, with an angiosarcoma of the skull base.
  • [MeSH-major] Hemangiosarcoma / diagnosis. Skull Base Neoplasms / diagnosis

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  • (PMID = 19716184.001).
  • [ISSN] 1872-8464
  • [Journal-full-title] International journal of pediatric otorhinolaryngology
  • [ISO-abbreviation] Int. J. Pediatr. Otorhinolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Ireland
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12. den Hoed ID, Granzen B, Granzen B, Aronson DC, Pauwels P, de Kraker J, van Heurn LW: Metastasized angiosarcoma of the spleen in a 2-year-old girl. Pediatr Hematol Oncol; 2005 Jul-Aug;22(5):387-90
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  • [Title] Metastasized angiosarcoma of the spleen in a 2-year-old girl.
  • Primary angiosarcoma of the spleen is rare and the prognosis is very poor.
  • The authors present a 2-year-old girl with spontaneous rupture of splenic angiosarcoma.
  • [MeSH-major] Hemangiosarcoma / secondary. Liver Neoplasms / secondary. Splenic Neoplasms / pathology

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  • (PMID = 16020128.001).
  • [ISSN] 0888-0018
  • [Journal-full-title] Pediatric hematology and oncology
  • [ISO-abbreviation] Pediatr Hematol Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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13. Castro EC, Galambos C, Shaw PH, Ranganathan S: Primary mesenteric angiosarcoma in a child with associated lymphangiectasia: a case report. Pediatr Dev Pathol; 2008 Nov-Dec;11(6):482-6
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  • [Title] Primary mesenteric angiosarcoma in a child with associated lymphangiectasia: a case report.
  • By contrast, angiosarcoma in adults usually occurs in the extremities in conjunction with lymphedema.
  • Mesenteric angiosarcoma has only rarely been reported.
  • We report a child who presented to the emergency room with an acute abdomen and underwent emergency surgery for a mesenteric angiosarcoma with associated lymphangiectasia of the bowel and mesentery.
  • [MeSH-major] Hemangiosarcoma / secondary. Lymphangiectasis, Intestinal / pathology. Peritoneal Neoplasms / pathology

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  • (PMID = 19143455.001).
  • [ISSN] 1093-5266
  • [Journal-full-title] Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
  • [ISO-abbreviation] Pediatr. Dev. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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14. Gatcombe HG, Olson TA, Esiashvili N: Metastatic primary angiosarcoma of the breast in a pediatric patient with a complete response to systemic chemotherapy and definitive radiation therapy: case report and review of the literature. J Pediatr Hematol Oncol; 2010 Apr;32(3):192-4
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  • [Title] Metastatic primary angiosarcoma of the breast in a pediatric patient with a complete response to systemic chemotherapy and definitive radiation therapy: case report and review of the literature.
  • We present a case of a rare malignancy, primary breast angiosarcoma, in a 15-year-old girl.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Bone Neoplasms / therapy. Breast Neoplasms / therapy. Hemangiosarcoma / therapy. Mediastinal Neoplasms / therapy. Radiotherapy

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  • (PMID = 20186104.001).
  • [ISSN] 1536-3678
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
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15. Zambrano E, Pérez-Atayde AR, Ahrens W, Reyes-Múgica M: Pediatric sclerosing rhabdomyosarcoma. Int J Surg Pathol; 2006 Jul;14(3):193-9
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  • [Title] Pediatric sclerosing rhabdomyosarcoma.
  • Sclerosing rhabdomyosarcoma, a particular phenotypic variant of rhabdomyosarcoma initially described in the adult population, has emerged as a potential pitfall in the evaluation of pediatric sarcomas.
  • Because of its densely hyalinized collagenous matrix and its occasional expression of a pseudovascular pattern of growth, sclerosing rhabdomyosarcoma has been at times misdiagnosed as chondrosarcoma, osteosarcoma, or angiosarcoma.
  • We describe 3 pediatric patients with sclerosing rhabdomyosarcoma and provide a detailed description of its distinguishing pathologic features.

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  • (PMID = 16959698.001).
  • [ISSN] 1066-8969
  • [Journal-full-title] International journal of surgical pathology
  • [ISO-abbreviation] Int. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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16. Bacchi CE, Silva TR, Zambrano E, Plaza J, Suster S, Luzar B, Lamovec J, Pizzolitto S, Falconieri G: Epithelioid angiosarcoma of the skin: a study of 18 cases with emphasis on its clinicopathologic spectrum and unusual morphologic features. Am J Surg Pathol; 2010 Sep;34(9):1334-43
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  • [Title] Epithelioid angiosarcoma of the skin: a study of 18 cases with emphasis on its clinicopathologic spectrum and unusual morphologic features.
  • We report 18 cases of cutaneous angiosarcoma with predominant or exclusive epithelioid morphology.
  • Patients' ages ranged from 2 to 97 years, median 77.5 years; 2 were pediatric patients.
  • Our data show that epithelioid cutaneous angiosarcoma may have a broad morphological spectrum, raising interpretive challenges on microscopy.
  • [MeSH-major] Epithelioid Cells / pathology. Hemangiosarcoma / pathology. Skin Neoplasms / pathology

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  • (PMID = 20697249.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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17. Shehata BM, Fishman I, Collings MH, Wang J, Poulik JM, Ricketts RR, Parker PM, Heiss K, Bhatia AM, Worcester HD, Gow KW: Pseudoangiomatous stromal hyperplasia of the breast in pediatric patients: an underrecognized entity. Pediatr Dev Pathol; 2009 Nov-Dec;12(6):450-4
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  • [Title] Pseudoangiomatous stromal hyperplasia of the breast in pediatric patients: an underrecognized entity.
  • Grossly, it most often resembles fibroadenoma, but may commonly be confused with angiosarcoma and other types of benign vascular proliferations.
  • While PASH has been described in female and male adults since the mid-1980s, there have been only a few accounts in the pediatric population.
  • We present a series of 12 pediatric patients with PASH, including a 3-year-old male, who we believe to be the youngest patient to present with this entity.
  • Our series documents that PASH is not uncommon in pediatric breast pathology and delineates important differences between adult and pediatric presentations of this entity.

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  • (PMID = 19606909.001).
  • [ISSN] 1093-5266
  • [Journal-full-title] Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
  • [ISO-abbreviation] Pediatr. Dev. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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18. Al-Daraji WI, Makhlouf HR, Miettinen M, Montgomery EA, Goodman ZD, Marwaha JS, Fanburg-Smith JC: Primary gallbladder sarcoma: a clinicopathologic study of 15 cases, heterogeneous sarcomas with poor outcome, except pediatric botryoid rhabdomyosarcoma. Am J Surg Pathol; 2009 Jun;33(6):826-34
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  • [Title] Primary gallbladder sarcoma: a clinicopathologic study of 15 cases, heterogeneous sarcomas with poor outcome, except pediatric botryoid rhabdomyosarcoma.
  • BACKGROUND: Primary gallbladder sarcoma (PGBS) is rare, with only 39 documented cases, with the predominant type being leiomyosarcoma.
  • DESIGN: Cases recorded as "gallbladder sarcoma" were retrieved from our files; the clinicopathologic features were reviewed and recorded.
  • Epithelial tumors, mixed tumors (carcinosarcoma or sarcomatoid carcinoma), tumors extending into the gallbladder from the abdomen, or sarcoma with other known primaries were excluded.
  • PGBSs were diagnosed as 7 myxofibrosarcomas [malignant fibrous histiocytoma, storiform pleomorphic to myxoid, 2 with an unusual fibromyxoid sarcoma-like (Evans-like), and pleomorphic hyalinizing angiectatic tumor-like mixture], 2 leiomyosarcomas, 1 gastrointestinal stromal tumor-like (GIST-like), 3 botryoid embryonal rhabdomyosarcomas (RMS), and 2 epithelioid angiosarcomas.
  • The GIST-like sarcoma was palisaded and myoid-like but failed to stain for CD34 or CD117.
  • A variety of sarcoma types are found, yet malignant fibrous histiocytoma is the predominant variant, more common than LMS.
  • GIST is a controversial sarcoma in gallbladder; angiosarcoma can rarely occur in this location.
  • [MeSH-major] Gallbladder Neoplasms / pathology. Sarcoma / pathology

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  • (PMID = 19194282.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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19. Meyers RL: Tumors of the liver in children. Surg Oncol; 2007 Nov;16(3):195-203
MedlinePlus Health Information. consumer health - Liver Cancer.

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  • In this review we examine the diagnosis and treatment of pediatric liver tumors- both malignant and benign.
  • Other malignant liver tumors are quite rare and include biliary rhabdomyosarcoma, angiosarcoma, rhabdoid tumor, and undifferentiated sarcoma.

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  • (PMID = 17714939.001).
  • [ISSN] 0960-7404
  • [Journal-full-title] Surgical oncology
  • [ISO-abbreviation] Surg Oncol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Netherlands
  • [Number-of-references] 69
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20. Nazir Z, Pervez S: Malignant vascular tumors of liver in neonates. J Pediatr Surg; 2006 Jan;41(1):e49-51
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  • The other neonate presented with intractable ascites and liver biopsy showed histological features of angiosarcoma.
  • Ascites has rarely been reported as a presenting feature of angiosarcoma in literature.
  • [MeSH-major] Hemangioendothelioma / pathology. Hemangiosarcoma / pathology. Liver Neoplasms / pathology

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  • (PMID = 16410090.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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21. Fresneau B, Oberlin O, Brugières L, Valteau-Couanet D, Patte C: [Malignant primary cardiac tumors in childhood and adolescence]. Arch Pediatr; 2010 May;17(5):495-501

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Malignant primary cardiac tumors in childhood and adolescence].
  • Among malignant cardiac tumors, sarcoma (rhabdomyosarcoma, angiosarcoma, synovial sarcoma) and lymphoma (Burkitt's lymphoma, large B-cell lymphoma, lymphoblastic lymphoma) predominate.
  • There are few published pediatric series on malignant primary cardiac tumors.
  • We report here 3 observations of primary malignant cardiac tumors, 2 cases of sarcoma (angiosarcoma and synovial sarcoma) and 1 case of Burkitt's lymphoma.
  • For sarcoma, treatment associates surgery and chemotherapy.
  • Surgery should be as complete as possible because of the lack of chemotherapy sensitivity of some sarcomas, mainly angiosarcoma and synovial sarcoma.
  • Therefore, the prognosis of cardiac sarcoma remains poor.
  • Prognosis depends on histology and not lymphoma location, and so is better than the prognosis for sarcoma.
  • [MeSH-major] Burkitt Lymphoma / diagnosis. Heart Neoplasms / diagnosis. Hemangiosarcoma / diagnosis. Sarcoma, Synovial / diagnosis

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  • [Copyright] Copyright 2010 Elsevier Masson SAS. All rights reserved.
  • (PMID = 20338733.001).
  • [ISSN] 1769-664X
  • [Journal-full-title] Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie
  • [ISO-abbreviation] Arch Pediatr
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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22. Blankenburg F, Scheer I, Sarioglu N, Henze G, Driever PH, Riebel T: Spontaneous regression of a vascular tumor of the skull base--infantile hemangioendothelioma? J Pediatr Hematol Oncol; 2008 Sep;30(9):712-5
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  • Histopathologically, vessel malformation, epitheloid hemangioendothelioma, and angiosarcoma were possible diagnoses.

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  • (PMID = 18776768.001).
  • [ISSN] 1536-3678
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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23. Ross JA: Environmental and genetic susceptibility to MLL-defined infant leukemia. J Natl Cancer Inst Monogr; 2008;(39):83-6
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The study of rare cancers, including retinoblastoma, angiosarcoma, and vaginal clear cell carcinoma, has contributed greatly to our understanding of cancer mechanisms.

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  • (PMID = 18648010.001).
  • [ISSN] 1052-6773
  • [Journal-full-title] Journal of the National Cancer Institute. Monographs
  • [ISO-abbreviation] J. Natl. Cancer Inst. Monographs
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA79940; United States / NCI NIH HHS / CA / U10 CA098543
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 149025-06-9 / Myeloid-Lymphoid Leukemia Protein
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24. Al Dhaybi R, Agoumi M, Powell J, Dubois J, Kokta V: Lymphangiosarcoma complicating extensive congenital mixed vascular malformations. Lymphat Res Biol; 2010 Sep;8(3):175-9
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  • Pediatric hepatic angiosarcoma is a very rare malignant vascular tumor.
  • A few cases have shown pediatric hepatic angiosarcoma occurring on a background of preexisting vascular lesions.
  • The autopsy's pathological examination revealed a hepatic-based angiosarcoma with plurimetastatic dissemination to the spleen, lungs, peritoneum, pleura, mesenteric linings as well as the serosa of the stomach and small intestine.
  • We hypothesize that these multiple extensive mixed vascular malformations were associated with chronic lymphedema which probably predisposed to the development of the angiosarcoma in our patient.

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  • (PMID = 20863270.001).
  • [ISSN] 1557-8585
  • [Journal-full-title] Lymphatic research and biology
  • [ISO-abbreviation] Lymphat Res Biol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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25. Moore SW, Davidson A, Hadley GP, Kruger M, Poole J, Stones D, Wainwright L, Wessels G: Malignant liver tumors in South African children: a national audit. World J Surg; 2008 Jul;32(7):1389-95
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Malignant liver tumors (mostly hepatoblastoma [HB] and hepatocellular carcinoma [HCC]) are uncommon, representing 0.5%-2% of childhood malignancies worldwide.
  • METHODS: Data were obtained from the tumor registry and pediatric oncology units in South African hospitals to audit and review the epidemiology, treatment, and outcome of malignant hepatic tumors in South African children.
  • Vascular tumors included hemangioendotheliomas (12), and there were 5 malignant tumors in children with HIV, including 1 angiosarcoma and 13 Kaposi sarcoma-like tumors.
  • Hepatic sarcoma occurred at a mean age of 7.66 years and had a female predominance (M:F ratio: 0.4).
  • There appeared to be an increase in the incidence of vascular tumors, presumably the result of an increase in Kaposi-like sarcoma in retrovirus-positive patients.

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  • (PMID = 18305988.001).
  • [ISSN] 0364-2313
  • [Journal-full-title] World journal of surgery
  • [ISO-abbreviation] World J Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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26. Raghu AR, Tandon S, Rao NN, Singh R, Rekha VK: Intraoral papillary endothelial hyperplasia: case discussion with supportive histochemistry and immunohistochemistry. J Clin Pediatr Dent; 2005;29(3):253-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Histologically, the tissue was characterized by the unusual endothelial cell proliferation, which is significant, as papillary endothelial hyperplasia resembles angiosarcoma and possible over-treatment thereafter.

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  • (PMID = 15926444.001).
  • [ISSN] 1053-4628
  • [Journal-full-title] The Journal of clinical pediatric dentistry
  • [ISO-abbreviation] J Clin Pediatr Dent
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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27. Zhang W, He J, Wang J, Bai H, Zhang X, Zhang G, Ren Y, Wang K, Xu J, Niu L, Zhou Y, Chen W: Ulcerated epithelioid hemangioendothelioma of the right armpit in childhood. J Pediatr Hematol Oncol; 2009 Aug;31(8):595-8
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  • [Title] Ulcerated epithelioid hemangioendothelioma of the right armpit in childhood.
  • Although the tumor is classified in between an angiolymphoid hyperplasia with eosinophilia and an epithelioid angiosarcoma, it sometimes takes a clinical course resembling that of angiosarcoma.

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  • (PMID = 19636267.001).
  • [ISSN] 1536-3678
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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