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Items 1 to 48 of about 48
1. Al-Za'abi AM, Ghazarian D, Greenberg GR, Shaw JC: Eruptive tufted angiomas in a patient with Crohn's disease. J Clin Pathol; 2005 Feb;58(2):214-6
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  • [Title] Eruptive tufted angiomas in a patient with Crohn's disease.
  • Angioblastoma is a rare, benign vascular tumour composed of undifferentiated mesenchymal cells with a tendency to form lumina.
  • This entity was first described by Nakagawa in 1949 as angioblastoma, and Wilson Jones was the first to use the term "tufted angioma" in 1976.
  • Tufted angiomas usually occur in infancy and spread slowly.
  • He developed numerous small itchy erythematous vascular appearing papules, which on histological examination resembled tufted angiomas, showing the classic "cannon ball" appearance.
  • This case may represent an eruptive acquired tufted angioma in which immunosuppression or drug induced modification of angiogenesis played a role in its development and regression.
  • One previous case of eruptive tufted angioma has been reported in an immunosuppressed patient.
  • [MeSH-major] Crohn Disease / pathology. Hemangioma / pathology. Skin Neoplasms / pathology

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  • [Cites] Dermatology. 2000;201(1):68-70 [10971067.001]
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  • [Cites] Clin Exp Dermatol. 1994 Nov;19(6):511-4 [7889677.001]
  • [Cites] Clin Exp Dermatol. 2000 Nov;25(8):627-30 [11167978.001]
  • (PMID = 15677546.001).
  • [ISSN] 0021-9746
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Gastrointestinal Agents; B72HH48FLU / Infliximab
  • [Other-IDs] NLM/ PMC1770572
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2. Kim T, Roh MR, Cho S, Chung KY: Kasabach-merritt syndrome arising from tufted angioma successfully treated with systemic corticosteroid. Ann Dermatol; 2010 Nov;22(4):426-30

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Kasabach-merritt syndrome arising from tufted angioma successfully treated with systemic corticosteroid.
  • We report a case of Kasabach-Merritt syndrome arising from a tufted angioma successfully treated with systemic corticosteroid.
  • The lesion was diagnosed as tufted angioma histopathologically.

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  • (PMID = 21165213.001).
  • [ISSN] 2005-3894
  • [Journal-full-title] Annals of dermatology
  • [ISO-abbreviation] Ann Dermatol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2991720
  • [Keywords] NOTNLM ; Kasabach-Merritt syndrome / Systemic corticosteroid / Tufted angioma
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3. Almaraz RL, Gutiérrez JC, Bieler CB, Hernández AH, González ME, Villar GR: [Infantile vascular tumors]. An Pediatr (Barc); 2010 Feb;72(2):143.e1-143.e15
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  • [Transliterated title] Tumores vasculares en la infancia.
  • Hemangiomas of infancy are by far the most frequent, and other less common types are congenital hemangiomas (rapidly involuting or RICH and non-involuting or NICH), kaposiform hemangioendothelioma, angioblastoma or tufted angioma and pyogenic granuloma.

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  • (PMID = 20022827.001).
  • [ISSN] 1695-9531
  • [Journal-full-title] Anales de pediatría (Barcelona, Spain : 2003)
  • [ISO-abbreviation] An Pediatr (Barc)
  • [Language] spa
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Spain
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4. Browning J, Frieden I, Baselga E, Wagner A, Metry D: Congenital, self-regressing tufted angioma. Arch Dermatol; 2006 Jun;142(6):749-51
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  • [Title] Congenital, self-regressing tufted angioma.
  • BACKGROUND: Tufted angioma (known in Japanese literature as angioblastoma of Nakagawa) is an uncommon, histologically benign, vascular tumor.
  • OBSERVATIONS: We present a series of 5 histopathologically confirmed cases of congenital tufted angioma that spontaneously regressed during infancy or early childhood.
  • CONCLUSION: We recommend that observation for potential regression be considered for otherwise uncomplicated congenital or early infantile cases of tufted angioma.
  • [MeSH-major] Hemangioma, Capillary / diagnosis. Neoplasm Regression, Spontaneous / pathology. Skin Neoplasms / diagnosis

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  • (PMID = 16785378.001).
  • [ISSN] 0003-987X
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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5. Sarma N, Das S, Roy AK: Annular tufted angioma. Indian J Dermatol Venereol Leprol; 2007 Nov-Dec;73(6):435-6
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  • [Title] Annular tufted angioma.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 18032876.001).
  • [ISSN] 0973-3922
  • [Journal-full-title] Indian journal of dermatology, venereology and leprology
  • [ISO-abbreviation] Indian J Dermatol Venereol Leprol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] India
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6. Reddy IS, Anuradha SV, Swarnalata G: Congenital giant tufted angioma. Indian J Dermatol Venereol Leprol; 2009 Nov-Dec;75(6):639
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  • [Title] Congenital giant tufted angioma.
  • [MeSH-major] Hemangioma / pathology. Neoplasms / pathology. Severity of Illness Index. Skin Neoplasms / pathology

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  • (PMID = 19915265.001).
  • [ISSN] 0973-3922
  • [Journal-full-title] Indian journal of dermatology, venereology and leprology
  • [ISO-abbreviation] Indian J Dermatol Venereol Leprol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] India
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7. Rohana AG, Norazmi MK, Norlaila M: A rare case of Von Hippel Lindau disease. Med J Malaysia; 2006 Jun;61(2):254-7
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  • VHL is associated with multi-organ involvement of benign and malignant tumours characterized by the presence of retinal angiomas, hemangioblastomas of the cerebellum and spinal cord, renal cell carcinomas, pheochromocytomas and other cystic lesions in the kidneys, pancreas, and epididymis.
  • It is a rare disorder with prevalence estimated at 2-3 per 100,000.
  • This case report describes a 37 years old Chinese gentleman who presented to our institution for further management of bilateral pheochromocytoma and retinal angioblastoma with problems of duodenal ulcer and anaemia.

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  • (PMID = 16898326.001).
  • [ISSN] 0300-5283
  • [Journal-full-title] The Medical journal of Malaysia
  • [ISO-abbreviation] Med. J. Malaysia
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Malaysia
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8. Schaffer JV, Fangman W, Bossenbroek NM, Meehan SA, Kamino H: Tufted angioma. Dermatol Online J; 2008;14(10):20
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma.
  • Histopathologic evaluation showed multiple, discrete lobules of tightly packed capillaries in a 'cannonball' pattern within the dermis, which confirmed the diagnosis of tufted angioma.
  • The clinical and histopathologic features, natural history, and treatment options for tufted angiomas are reviewed; their relationship to kaposiform hemangioendotheliomas is discussed.
  • [MeSH-major] Hemangioma / diagnosis. Skin Neoplasms / diagnosis


9. Na JI, Cho KH, Kim YG, Park KC: Angioblastoma showing aggravation after treatment with long-pulsed Nd:YAG laser (1064 nm). Pediatr Dermatol; 2007 Jul-Aug;24(4):397-400
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  • [Title] Angioblastoma showing aggravation after treatment with long-pulsed Nd:YAG laser (1064 nm).
  • Angioblastoma usually develops in infancy or early childhood on the neck or upper trunk.
  • It is known to be slowly progressive and benign in nature, but treatment guidelines have not yet been established.
  • We report this occurrence to increase awareness of trauma-induced aggravation phenomena in angioblastoma.
  • [MeSH-major] Hemangioblastoma / pathology. Hemangioblastoma / radiotherapy. Lasers / adverse effects. Skin Neoplasms / pathology. Skin Neoplasms / radiotherapy

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  • (PMID = 17845165.001).
  • [ISSN] 1525-1470
  • [Journal-full-title] Pediatric dermatology
  • [ISO-abbreviation] Pediatr Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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10. Mao RJ, Li QM, Guo YM, Li WQ, Fan CS, Zhu XZ: [Clinicopathologic study of giant cell angioblastoma]. Zhonghua Bing Li Xue Za Zhi; 2010 Nov;39(11):752-6
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  • [Title] [Clinicopathologic study of giant cell angioblastoma].
  • OBJECTIVE: to study the clinicopathological features, imaging characteristics, immunophenotypes and differential diagnosis of giant cell angioblastoma (GCAB).
  • A concentric arrangement of oval-to-spindle Cells around small-caliber vascular structures together with collagen fiber contributed to a so-called 'onion-skin' arrangement.
  • CONCLUSION: GCAB is a rare, locally infiltrative but slow growing neoplastic angiogenesis with unique morphological characteristics during infancy, which may occur not only in the skin, mucosa, subcutis and deep soft tissue but also in the bone.
  • [MeSH-minor] Actins / metabolism. Antigens, CD / metabolism. Antigens, CD31 / metabolism. Antigens, CD34 / metabolism. Antigens, Differentiation, Myelomonocytic / metabolism. Dermatofibrosarcoma / metabolism. Dermatofibrosarcoma / pathology. Diagnosis, Differential. Fibula. Hemangioendothelioma / metabolism. Hemangioendothelioma / pathology. Hemangioendothelioma, Epithelioid / metabolism. Hemangioendothelioma, Epithelioid / pathology. Hemangioma, Cavernous / metabolism. Hemangioma, Cavernous / pathology. Humans. Infant. Kasabach-Merritt Syndrome. Male. Sarcoma, Kaposi / metabolism. Sarcoma, Kaposi / pathology. Skin Neoplasms / metabolism. Skin Neoplasms / pathology. Thrombocytopenia / metabolism. Thrombocytopenia / pathology. Tomography, X-Ray Computed. Vascular Neoplasms / metabolism. Vascular Neoplasms / pathology. Vimentin / metabolism

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  • (PMID = 21215166.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / ACTA2 protein, human; 0 / Actins; 0 / Antigens, CD; 0 / Antigens, CD31; 0 / Antigens, CD34; 0 / Antigens, Differentiation, Myelomonocytic; 0 / CD68 antigen, human; 0 / Vimentin; Kaposiform Hemangioendothelioma
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11. Chiu CS, Yang LC, Hong HS, Kuan YZ: Treatment of a tufted angioma with intense pulsed light. J Dermatolog Treat; 2007;18(2):109-11
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  • [Title] Treatment of a tufted angioma with intense pulsed light.
  • Tufted angioma is a rare cutaneous angiomatous proliferation named because of its characteristic histologic pattern of grouped dermal capillary tufts.
  • Although transformation to malignancy has not been described, tufted angiomas do not tend to regress.
  • We report an adult case of tufted angioma, with unusual presentation as annular plaques, which was alleviated after treatment with intense pulsed light in terms of both cosmetics and discomfort.
  • [MeSH-major] Hemangioma / diagnosis. Hemangioma / therapy. Skin Neoplasms / diagnosis. Skin Neoplasms / therapy

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  • (PMID = 17520468.001).
  • [ISSN] 0954-6634
  • [Journal-full-title] The Journal of dermatological treatment
  • [ISO-abbreviation] J Dermatolog Treat
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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12. Arai E, Kuramochi A, Tsuchida T, Tsuneyoshi M, Kage M, Fukunaga M, Ito T, Tada T, Izumi M, Shimizu K, Hirose T, Shimizu M: Usefulness of D2-40 immunohistochemistry for differentiation between kaposiform hemangioendothelioma and tufted angioma. J Cutan Pathol; 2006 Jul;33(7):492-7
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  • [Title] Usefulness of D2-40 immunohistochemistry for differentiation between kaposiform hemangioendothelioma and tufted angioma.
  • Our objective was to elucidate, using D2-40 immunohistochemistry, the differences among capillary hemangiomas, and especially between kaposiform hemangioendothelioma (KHE) and tufted angioma (TA).
  • In addition, the difference of immunostaining pattern of D2-40 is limited to the peripheral area of capillary proliferation and surrounding dilated vessels; therefore, it is suggested that KHE and TA may reflect different stages in the evolution of a single entity.
  • [MeSH-major] Antibodies, Monoclonal / immunology. Biomarkers, Tumor / immunology. Hemangioendothelioma / diagnosis. Hemangioma / diagnosis. Sarcoma, Kaposi / diagnosis. Skin Neoplasms / diagnosis


13. Ramesh R, De Silva B, Atherton DJ: Congenital tufted angioma with persistent low-grade coagulopathy. Clin Exp Dermatol; 2009 Dec;34(8):e766-8
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  • [Title] Congenital tufted angioma with persistent low-grade coagulopathy.
  • A female infant, born with a tufted angioma, developed a coagulopathy with prolonged bleeding time, with the risk of progression to Kasabach-Merritt phenomenon.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 19778314.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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14. Bienaimé A, Rojat-Habib MC, Hesse S, Pelissier JF, Bonerandi JJ: [Giant vascular tumour in an adult: tufted angioma or kaposiform hemangioendothelioma]. Ann Dermatol Venereol; 2006 Jun-Jul;133(6-7):553-6
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  • [Title] [Giant vascular tumour in an adult: tufted angioma or kaposiform hemangioendothelioma].
  • [Transliterated title] Tumeur vasculaire géante de l'adulte: angiome en touffe ou hémangioendothéliome kaposiforme.
  • INTRODUCTION: Tufted angioma and kaposiform hemangioendothelioma are two rare benign but aggressive vascular tumours that occur mainly in children.
  • On histological examination there were features of tufted angioma and kaposiform hemangioendothelioma.
  • The histological association of aspects which could correspond to tufted angioma and kaposiform hemangioendothelioma seems to confirm recent publications which support the hypothesis that these two tumours are two evolutive stages of one and only entity.
  • [MeSH-major] Hemangioendothelioma / pathology. Hemangioma / pathology. Skin Neoplasms / pathology


15. Fahrtash F, McCahon E, Arbuckle S: Successful treatment of kaposiform hemangioendothelioma and tufted angioma with vincristine. J Pediatr Hematol Oncol; 2010 Aug;32(6):506-10
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  • [Title] Successful treatment of kaposiform hemangioendothelioma and tufted angioma with vincristine.
  • BACKGROUND: Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are rare, locally aggressive vascular tumors.
  • [MeSH-major] Antineoplastic Agents / therapeutic use. Hemangioendothelioma / drug therapy. Hemangioma / drug therapy. Vincristine / therapeutic use


16. Le Huu AR, Jokinen CH, Rubin BP, Mihm MC, Weiss SW, North PE, Dadras SS: Expression of prox1, lymphatic endothelial nuclear transcription factor, in Kaposiform hemangioendothelioma and tufted angioma. Am J Surg Pathol; 2010 Nov;34(11):1563-73
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  • [Title] Expression of prox1, lymphatic endothelial nuclear transcription factor, in Kaposiform hemangioendothelioma and tufted angioma.
  • Kaposiform hemangioendothelioma (KHE) and tufted angioma (TA) are rare tumors mainly occurring in early childhood.
  • For this purpose, we examined 75 vascular lesions: KHE (n=18), TA (n=13), infantile hemangioma (n=13), pyogenic granuloma (n=18), and granulation tissue (n=13).
  • Overall, our results show, for the first time, that Prox1 is an immunohistochemical biomarker helpful in confirming the diagnosis of KHE/TA and in distinguishing it from infantile hemangioma and pyogenic granuloma.
  • [MeSH-major] Biomarkers, Tumor / analysis. Hemangioendothelioma / chemistry. Hemangioma / chemistry. Homeodomain Proteins / analysis. Skin Neoplasms / chemistry. Soft Tissue Neoplasms / chemistry. Tumor Suppressor Proteins / analysis

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  • [ErratumIn] Am J Surg Pathol. 2011 Feb;35(2):314. Ruben, Brian P [corrected to Rubin, Brian P]
  • (PMID = 20975337.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD31; 0 / Antigens, CD34; 0 / Biomarkers, Tumor; 0 / Homeodomain Proteins; 0 / LYVE1 protein, human; 0 / Membrane Glycoproteins; 0 / PDPN protein, human; 0 / Tumor Suppressor Proteins; 0 / Vesicular Transport Proteins; 0 / prospero-related homeobox 1 protein
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17. Ishikawa K, Hatano Y, Ichikawa H, Hashimoto H, Fujiwara S: The spontaneous regression of tufted angioma. A case of regression after two recurrences and a review of 27 cases reported in the literature. Dermatology; 2005;210(4):346-8
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  • [Title] The spontaneous regression of tufted angioma. A case of regression after two recurrences and a review of 27 cases reported in the literature.
  • BACKGROUND: Tufted angioma, a peculiar angioma that is characterized by tufts of capillary-sized vessels scattered 'cannonball fashion' within the dermis, is known, on occasion, to regress spontaneously.
  • OBJECTIVE: To know the appropriate waiting period for spontaneous regression of tufted angioma.
  • METHODS: We report here a case of tufted angioma that regressed spontaneously after the lesions had recurred twice.
  • We also review previously reported cases of tufted angioma with spontaneous regression, including cases in the Japanese and non-Japanese literature.
  • [MeSH-major] Hemangioma, Capillary / pathology. Neoplasm Regression, Spontaneous / pathology. Skin Neoplasms / pathology

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  • [Copyright] 2005 S. Karger AG, Basel
  • (PMID = 15942226.001).
  • [ISSN] 1018-8665
  • [Journal-full-title] Dermatology (Basel, Switzerland)
  • [ISO-abbreviation] Dermatology (Basel)
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Switzerland
  • [Number-of-references] 10
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18. Alberola FT, Betlloch I, Montero LC, Nortes IB, Martínez NL, Paz AM: Congenital tufted angioma: Case report and review of the literature. Dermatol Online J; 2010;16(5):2
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  • [Title] Congenital tufted angioma: Case report and review of the literature.
  • Tufted angiomas (TA) are rare benign vascular tumors of unknown pathogenesis.
  • Tufted angiomas have a characteristic histology consisting of a proliferation of endothelial cells forming lobules with the typical "shotgun" distribution.
  • [MeSH-major] Hemangioma / congenital. Skin Neoplasms / congenital

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  • (PMID = 20492819.001).
  • [ISSN] 1087-2108
  • [Journal-full-title] Dermatology online journal
  • [ISO-abbreviation] Dermatol. Online J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 24
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19. Lee B, Chiu M, Soriano T, Craft N: Adult-onset tufted angioma: a case report and review of the literature. Cutis; 2006 Nov;78(5):341-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult-onset tufted angioma: a case report and review of the literature.
  • Tufted angiomas (TAs) are benign vascular tumors, primarily occurring on the trunk and extremities of children younger than 5 years.
  • [MeSH-major] Hemangioma / pathology. Lip Neoplasms / pathology. Skin Neoplasms / pathology


20. Goh SG, Calonje E: Cutaneous vascular tumours: an update. Histopathology; 2008 May;52(6):661-73
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  • This review evaluates changes in vascular nomenclature particularly in the category of vascular tumours of intermediate malignancy that includes the various haemangioendotheliomas, Kaposi's sarcoma and giant cell angioblastoma.
  • [MeSH-major] Neoplasms, Vascular Tissue / classification. Neoplasms, Vascular Tissue / pathology. Skin Neoplasms / classification. Skin Neoplasms / pathology
  • [MeSH-minor] Diagnosis, Differential. Hemangioendothelioma / diagnosis. Hemangioendothelioma / pathology. Hemangioma / diagnosis. Hemangioma / pathology. Humans. Lymphangioma / diagnosis. Lymphangioma / pathology. Soft Tissue Neoplasms / diagnosis. Soft Tissue Neoplasms / pathology

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  • (PMID = 18266723.001).
  • [ISSN] 1365-2559
  • [Journal-full-title] Histopathology
  • [ISO-abbreviation] Histopathology
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 69
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21. Osio A, Fraitag S, Hadj-Rabia S, Bodemer C, de Prost Y, Hamel-Teillac D: Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literature. Arch Dermatol; 2010 Jul;146(7):758-63
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literature.
  • BACKGROUND: Tufted angioma (TA) is a rare benign vascular tumor that mostly appears during infancy or early childhood.
  • [MeSH-major] Hemangioma / pathology. Skin / pathology. Skin Neoplasms / pathology

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  • (PMID = 20644037.001).
  • [ISSN] 1538-3652
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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22. Henriquez F, Gallego R, Oliva E, Silva D, Vega N: Conversion to rapamycin in a renal transplant patient with von Hippel-Lindau disease: encouraging results-a case report. Transplant Proc; 2008 Nov;40(9):3115-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Herein we have presented a case in which conversion to sirolimus improved graft function and also caused regression of retinal angioblastomas.

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  • (PMID = 19010210.001).
  • [ISSN] 0041-1345
  • [Journal-full-title] Transplantation proceedings
  • [ISO-abbreviation] Transplant. Proc.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Immunosuppressive Agents; W36ZG6FT64 / Sirolimus
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23. Drabko K, Choma M, Zaucha-Prazmo A, Wójcik B, Gorczyńska E, Kałwak K, Turkiewicz D, Słociak M, Ussowicz M, Dyla A, Chybicka A, Styczyński J, Debski R, Wysocki M, Goździk J, Ratajczak M, Kowalczyk JR: [Megachemotherapy and autologous hematopoietic stem cell transplantation in children with solid tumours excluding neuroblastoma--experience of Polish paediatric centres]. Med Wieku Rozwoj; 2006 Jul-Sep;10(3 Pt 1):785-92
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • 25 children were treated for Ewing Sarcoma, 13 for rhabdomyosarcoma embryonale (RMS), 7 for germinal tumours, 6 for medulloblastoma, 4 for PNET, 4 for Wilm's tumours, 2 for glioblastoma and single patients with mesenchymoma, astrocytoma, ependymoma, angioblastoma, carcinoma ovarian and carcinoma embryonale glutei.
  • One toxic death was noted--it was a boy, transplanted with progressive disease.

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  • (PMID = 17317909.001).
  • [Journal-full-title] Medycyna wieku rozwojowego
  • [ISO-abbreviation] Med Wieku Rozwoj
  • [Language] pol
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Poland
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Alkylating
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24. da Silva EB Jr, Leal AG, Milano JB, da Silva LF Jr, Clemente RS, Ramina R: Image-guided surgical planning using anatomical landmarks in the retrosigmoid approach. Acta Neurochir (Wien); 2010 May;152(5):905-10

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • RESULTS: There were 19 cases of vestibular schwannomas, 5 petroclival meningiomas, 3 trigeminal neuralgias, 1 angioblastoma, 1 epidermoid cyst and 1 hemifacial spasm.

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  • (PMID = 19902141.001).
  • [ISSN] 0942-0940
  • [Journal-full-title] Acta neurochirurgica
  • [ISO-abbreviation] Acta Neurochir (Wien)
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Austria
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25. Fernandez-Pineda I, Lopez-Gutierrez JC, Ramirez G, Marquez C: Vincristine-ticlopidine-aspirin: an effective therapy in children with Kasabach-Merritt phenomenon associated with vascular tumors. Pediatr Hematol Oncol; 2010 Nov;27(8):641-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Kasabach-Merritt phenomenon (KMP) is a serious coagulopathy with severe thrombocytopenia (<10,000/mm³) that occurs in the presence of an enlarging vascular tumor such as kaposiform hemangioendothelioma (KHE) and tufted angioma (TA).
  • [MeSH-minor] Disseminated Intravascular Coagulation / complications. Disseminated Intravascular Coagulation / diagnosis. Disseminated Intravascular Coagulation / drug therapy. Female. Hemangioma, Capillary / complications. Hemangioma, Capillary / diagnosis. Hemangioma, Capillary / drug therapy. Humans. Infant. Kasabach-Merritt Syndrome. Treatment Outcome

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  • (PMID = 20863161.001).
  • [ISSN] 1521-0669
  • [Journal-full-title] Pediatric hematology and oncology
  • [ISO-abbreviation] Pediatr Hematol Oncol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; OM90ZUW7M1 / Ticlopidine; R16CO5Y76E / Aspirin
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26. Enjolras O, Picard A, Soupre V: [Congenital haemangiomas and other rare infantile vascular tumours]. Ann Chir Plast Esthet; 2006 Aug-Oct;51(4-5):339-46
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Tufted angioma and kaposiform haemangioendothelioma are histopathologically well characterized; in addition they are now considered as part of a same spectrum of vascular tumours, with the contribution of lymphatic endothelial cells in their proliferation.
  • [MeSH-major] Hemangioma / congenital. Neoplasms, Vascular Tissue / diagnosis. Skin Neoplasms / congenital
  • [MeSH-minor] Biomarkers, Tumor / analysis. Blood Platelets / pathology. Child. Disseminated Intravascular Coagulation / diagnosis. Glucose Transporter Type 1 / analysis. Hemangioendothelioma / diagnosis. Hemangioma, Capillary / congenital. Humans. Infant. Prognosis. Remission, Spontaneous. Syndrome. Thrombocytopenia / diagnosis

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  • (PMID = 16997442.001).
  • [ISSN] 0294-1260
  • [Journal-full-title] Annales de chirurgie plastique et esthétique
  • [ISO-abbreviation] Ann Chir Plast Esthet
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Glucose Transporter Type 1; 0 / SLC2A1 protein, human
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27. Liu XJ, Tai MZ, Tian MX, Qin ZP: [Clinical analysis of 17 cases of pneumatic compression therapy in infants with Kasabach-Merritt phenomenon]. Zhonghua Yi Xue Za Zhi; 2009 Jul 14;89(26):1830-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The self-designed device for pneumatic compression hemangioma therapy was employed (Patent No: ZL97232266. 3).
  • There were 14 cases of kaposiform hemangioendothelioma (KHE) and 3 cases of tufted hemangioma (TA).

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  • (PMID = 19953927.001).
  • [ISSN] 0376-2491
  • [Journal-full-title] Zhonghua yi xue za zhi
  • [ISO-abbreviation] Zhonghua Yi Xue Za Zhi
  • [Language] chi
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] China
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28. Gruman A, Liang MG, Mulliken JB, Fishman SJ, Burrows PE, Kozakewich HP, Blei F, Frieden IJ: Kaposiform hemangioendothelioma without Kasabach-Merritt phenomenon. J Am Acad Dermatol; 2005 Apr;52(4):616-22
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Kasabach-Merritt phenomenon is a serious coagulopathy associated with kaposiform hemangioendothelioma (KHE), tufted angioma, and possibly other vascular neoplasms.
  • KHE presenting in the absence of Kasabach-Merritt phenomenon is rare, although tufted angioma frequently occurs without thrombocytopenia.
  • The tumors appeared as soft tissue masses with the overlying skin being either normal, erythematous, or violaceous.
  • [MeSH-major] Hemangioendothelioma / diagnosis. Skin Neoplasms / diagnosis


29. Harper L, Michel JL, Enjolras O, Raynaud-Mounet N, Rivière JP, Heigele T, De Napoli-Cocci S: Successful management of a retroperitoneal kaposiform hemangioendothelioma with Kasabach-Merritt phenomenon using alpha-interferon. Eur J Pediatr Surg; 2006 Oct;16(5):369-72
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  • It has been shown recently that Kasabach-Merritt phenomenon, the association of a vascular tumour and consumption coagulopathy, does not--as previously thought--complicate "classical" infantile hemangiomas but distinctive entities called kaposiform hemangioendothelioma (KHE) and tufted angioma (TA), both tumours on the same neoplastic spectrum.

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  • (PMID = 17160787.001).
  • [ISSN] 0939-7248
  • [Journal-full-title] European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift für Kinderchirurgie
  • [ISO-abbreviation] Eur J Pediatr Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Angiogenesis Inhibitors; 0 / Interferon-alpha
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30. Rodriguez V, Lee A, Witman PM, Anderson PA: Kasabach-merritt phenomenon: case series and retrospective review of the mayo clinic experience. J Pediatr Hematol Oncol; 2009 Jul;31(7):522-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Kasabach-Merritt phenomenon (KMP) is a rare thrombocytopenic consumption coagulopathy associated with an enlarging tufted angioma or kaposiform hemangioendothelioma.
  • [MeSH-major] Disseminated Intravascular Coagulation / complications. Disseminated Intravascular Coagulation / physiopathology. Hemangioendothelioma / complications. Hemangioma / complications. Skin Neoplasms / complications

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  • (PMID = 19564750.001).
  • [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; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Anti-Inflammatory Agents; 0 / Antineoplastic Agents
  • [Number-of-references] 10
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31. Sidbury R: Update on vascular tumors of infancy. Curr Opin Pediatr; 2010 Aug;22(4):432-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Kaposiform hemangioendothelioma and tufted angioma are less common than IH but more often associated with coagulopathy (Kasabach-Merritt phenomenon).

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  • (PMID = 20601884.001).
  • [ISSN] 1531-698X
  • [Journal-full-title] Current opinion in pediatrics
  • [ISO-abbreviation] Curr. Opin. Pediatr.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Vasodilator Agents; 9Y8NXQ24VQ / Propranolol
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32. Enjolras O, Soupre V, Picard A: [Classification of superficial vascular anomalies]. Presse Med; 2010 Apr;39(4):457-64
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • All superficial vascular abnormalities are not angiomas even though this term continues - incorrectly - to be used.
  • Because the suffix "oma" implies a tumor, it is necessary to differentiate true vascular tumors, such as infantile hemangioma, from vascular malformations.
  • In addition to the functioning of the impaired or severely damaged vessels, we discuss slow-flow capillary, venous, or lymphatic malformations and rapid flow arterial and arteriovenous malformations.
  • Infantile hemangioma is by far the most frequent (8 to 10 children/100).
  • This immunophenotype is present in all cases of infantile hemangioma at every stage and is negative in other tumors.
  • Kasabach-Merritt syndrome and its accompanying severe thrombocytopenia never complicate childhood hemangioma, contrary to what has been said for nearly 60 years.
  • When it is present, the tumor is either a tufted angioma or kaposiform hemangioendothelioma, and the GLUT1 marker can distinguish them from infantile hemangioma if the histologic diagnosis is uncertain (GLUT 1 is negative in both the latter cases).
  • [MeSH-minor] Biomarkers, Tumor / analysis. Blood Coagulation Disorders / diagnosis. Diagnosis, Differential. Diagnostic Imaging. Glucose Transporter Type 1 / analysis. Hemangioma / diagnosis. Humans. Syndrome. Thrombocytopenia / diagnosis. Vascular Neoplasms / diagnosis

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  • [Copyright] (c) 2010. Published by Elsevier Masson SAS.
  • (PMID = 20206462.001).
  • [ISSN] 2213-0276
  • [Journal-full-title] Presse medicale (Paris, France : 1983)
  • [ISO-abbreviation] Presse Med
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Glucose Transporter Type 1
  • [Number-of-references] 30
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33. Al Dhaybi R, Powell J, McCuaig C, Kokta V: Differentiation of vascular tumors from vascular malformations by expression of Wilms tumor 1 gene: evaluation of 126 cases. J Am Acad Dermatol; 2010 Dec;63(6):1052-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • METHODS: Based on the International Society for the Study of Vascular Anomalies classification of vascular anomalies, we studied the expression of WT1 in vascular tumors composed of infantile hemangioma, congenital hemangiomas (non-involuting, rapidly involuting, and not otherwise specified), pyogenic granuloma, tufted angioma, cherry angioma, Kaposi sarcoma, and angiosarcoma.
  • We also studied WT1 expression in vascular malformations composed of angiokeratoma/verrucous hemangioma, combined vascular malformations, venous malformations, glomuvenous malformations, lymphatic malformations/lymphangioma, telangiectasia, and targetoid hemosiderotic hemangioma.
  • [MeSH-major] Arteriovenous Malformations / pathology. Biomarkers, Tumor / metabolism. Hemangioma / pathology. Nuclear Proteins / metabolism. Vascular Neoplasms / pathology

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  • [Copyright] Copyright © 2009 American Academy of Dermatology, Inc. Published by Mosby, Inc. All rights reserved.
  • (PMID = 21093662.001).
  • [ISSN] 1097-6787
  • [Journal-full-title] Journal of the American Academy of Dermatology
  • [ISO-abbreviation] J. Am. Acad. Dermatol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Nuclear Proteins; 0 / WTAP protein, human
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34. Galambos C, Nodit L: Identification of lymphatic endothelium in pediatric vascular tumors and malformations. Pediatr Dev Pathol; 2005 Mar-Apr;8(2):181-9
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  • The lymphatic lesions included 6 lymphatic malformations, 5 cystic hygromas (macrocystic lymphatic malformation), 2 lymphovenous malformations, and 1 lymphangioma, and the vascular lesions comprised 3 infantile hemangiomas, 3 Kaposiform hemangioendotheliomas, 2 tufted angiomas, 1 pyogenic granuloma, 1 arteriovenous, and 1 venulocapillary malformations.

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  • (PMID = 15719202.001).
  • [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
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Biomarkers
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35. Lee SJ, Shin DJ, Kim HY, Lee WJ, Kim DW, Chung HY, Baik SK, Lee JM, Huh S, Yoon GS: A fraction of deep vascular birthmarks are true deep hemangiomas of infancy. Int J Dermatol; 2009 Aug;48(8):817-21
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  • BACKGROUND: Deeply-located vascular birthmarks have been traditionally regarded as being identical to a deep type of hemangioma of infancy (HOI).
  • The remaining were comprised of 6 venous malformations (31.6%), 3 lymphatic malformations (15.8%), 1 glomangioma (5.3%) and 5 tufted angiomas (26.3%).
  • [MeSH-major] Hemangioma / pathology. Skin / blood supply. Skin / pathology. Vascular Malformations / pathology. Vascular Neoplasms / pathology

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  • (PMID = 19659859.001).
  • [ISSN] 1365-4632
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Murine-Derived; 0 / Antigens, CD31; 0 / Biomarkers, Tumor; 0 / Glucose Transporter Type 1; 0 / SLC2A1 protein, human; 0 / monoclonal antibody D2-40
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36. Guillou L: [Mesenchymal tumors of the skin. Tufted angioma (angioblastoma)]. Ann Pathol; 2009 Oct;29(5):416-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Mesenchymal tumors of the skin. Tufted angioma (angioblastoma)].
  • [Transliterated title] Tumeurs conjonctives de la peau. Cas n(o) 8. Hémangiome acquis en touffes (angioblastome de Nakagawa).
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 20004845.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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37. Kamath GH, Bhat RM, Kumar S: Tufted angioma. Int J Dermatol; 2005 Dec;44(12):1045-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 16409274.001).
  • [ISSN] 0011-9059
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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38. Kim CY, Nam YH, Kim GD, Oh CW: Tufted angioma in site of healed herpes zoster: isotopic response. Clin Exp Dermatol; 2006 Sep;31(5):714-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma in site of healed herpes zoster: isotopic response.
  • [MeSH-major] Hemangioma, Capillary / etiology. Herpes Zoster / complications. Skin Diseases, Viral / complications. Skin Neoplasms / etiology

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  • (PMID = 16901320.001).
  • [ISSN] 0307-6938
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
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39. Barco D, Baselga E, Ribé A, Alomar A: [Congenital self-limiting tufted angioma]. Actas Dermosifiliogr; 2008 Jun;99(5):423-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Congenital self-limiting tufted angioma].
  • [Transliterated title] Angioma en penacho congénito regresivo.
  • [MeSH-major] Arm. Hemangioma / congenital. Hemangioma / pathology. Neoplasm Regression, Spontaneous. Skin Neoplasms / congenital. Skin Neoplasms / pathology

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  • (PMID = 18501182.001).
  • [ISSN] 0001-7310
  • [Journal-full-title] Actas dermo-sifiliográficas
  • [ISO-abbreviation] Actas Dermosifiliogr
  • [Language] spa
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Spain
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40. Fujita H, Asahina A, Tamaki K: Extensive tufted angioma of the left arm in a 47-year-old woman. Clin Exp Dermatol; 2009 Oct;34(7):e216-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extensive tufted angioma of the left arm in a 47-year-old woman.
  • [MeSH-major] Arm. Hemangioma / diagnosis. Skin Neoplasms / diagnosis

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  • (PMID = 19323667.001).
  • [ISSN] 1365-2230
  • [Journal-full-title] Clinical and experimental dermatology
  • [ISO-abbreviation] Clin. Exp. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
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41. Khoo JJ, Choon SE: Childhood tufted angioma. Pathology; 2006 Jun;38(3):268-70
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Childhood tufted angioma.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 16753756.001).
  • [ISSN] 0031-3025
  • [Journal-full-title] Pathology
  • [ISO-abbreviation] Pathology
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
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42. Chakraborty S, Gharami RC, Das NK, Datta PK: Annular tufted angioma: a rare entity. Int J Dermatol; 2009 Jun;48(6):614-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Annular tufted angioma: a rare entity.
  • [MeSH-major] Dermis / blood supply. Dermis / pathology. Hemangioma / pathology. Vascular Neoplasms / pathology

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  • (PMID = 19538371.001).
  • [ISSN] 1365-4632
  • [Journal-full-title] International journal of dermatology
  • [ISO-abbreviation] Int. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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43. Ma HJ, Zhao G, Li Y, Li DG: Tufted angioma presented with segmental hyperpigmented plaque in a young Chinese woman. J Dermatol; 2010 Feb;37(2):190-2
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma presented with segmental hyperpigmented plaque in a young Chinese woman.
  • [MeSH-major] Hemangioma / diagnosis. Skin Neoplasms / diagnosis

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  • (PMID = 20175859.001).
  • [ISSN] 1346-8138
  • [Journal-full-title] The Journal of dermatology
  • [ISO-abbreviation] J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Vimentin
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44. Ferrandiz-Pulido C, Mollet J, Sabado C, Ferrer B, Garcia-Patos V: Tufted angioma associated with Kasabach-Merritt phenomenon: a therapeutic challenge. Acta Derm Venereol; 2010 Sep;90(5):535-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma associated with Kasabach-Merritt phenomenon: a therapeutic challenge.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Skin / drug effects
  • [MeSH-minor] Biopsy. Child, Preschool. Disseminated Intravascular Coagulation / blood. Disseminated Intravascular Coagulation / diagnosis. Disseminated Intravascular Coagulation / drug therapy. Disseminated Intravascular Coagulation / pathology. Female. Hemangioma / blood. Hemangioma / diagnosis. Hemangioma / drug therapy. Hemangioma / pathology. Hemangioma, Capillary / blood. Hemangioma, Capillary / diagnosis. Hemangioma, Capillary / drug therapy. Hemangioma, Capillary / pathology. Humans. Infant. Kasabach-Merritt Syndrome. Platelet Count. Skin Neoplasms / blood. Skin Neoplasms / diagnosis. Skin Neoplasms / drug therapy. Skin Neoplasms / pathology. Time Factors. Treatment Outcome

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  • (PMID = 20814640.001).
  • [ISSN] 1651-2057
  • [Journal-full-title] Acta dermato-venereologica
  • [ISO-abbreviation] Acta Derm. Venereol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Sweden
  • [Chemical-registry-number] Tufted angioma
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45. McAleer MA, Kirby B, Sheahan K, Collins P: An erythematous patch and plaque on the shoulder--quiz case. Acquired tufted angioma (TA). Arch Dermatol; 2008 Sep;144(9):1217-22
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] An erythematous patch and plaque on the shoulder--quiz case. Acquired tufted angioma (TA).
  • [MeSH-major] Hemangioma / pathology. Shoulder. Skin Neoplasms / pathology

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  • (PMID = 18794471.001).
  • [ISSN] 1538-3652
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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46. Yesudian PD, Parslew R, Klafowski J, Gould D, Pizer B: Tufted angioma-associated Kasabach-Merritt syndrome treated with embolization and vincristine. Plast Reconstr Surg; 2008 Feb;121(2):692-3
Hazardous Substances Data Bank. VINCRISTINE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma-associated Kasabach-Merritt syndrome treated with embolization and vincristine.
  • [MeSH-major] Antineoplastic Agents, Phytogenic / therapeutic use. Embolization, Therapeutic / methods. Hemangioendothelioma / therapy. Skin Neoplasms / therapy. Vincristine / therapeutic use

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  • (PMID = 18301012.001).
  • [ISSN] 1529-4242
  • [Journal-full-title] Plastic and reconstructive surgery
  • [ISO-abbreviation] Plast. Reconstr. Surg.
  • [Language] eng
  • [Publication-type] Letter
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Phytogenic; 5J49Q6B70F / Vincristine
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47. Yesudian PD, Klafkowski J, Parslew R, Gould D, Lloyd D, Pizer B: Tufted angioma-associated Kasabach-Merritt syndrome treated with embolization and vincristine. Plast Reconstr Surg; 2007 Apr 1;119(4):1392-3
Hazardous Substances Data Bank. VINCRISTINE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tufted angioma-associated Kasabach-Merritt syndrome treated with embolization and vincristine.
  • [MeSH-major] Embolization, Therapeutic / methods. Hemangioendothelioma / therapy. Skin Neoplasms / therapy. Vincristine / therapeutic use

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  • (PMID = 17496631.001).
  • [ISSN] 1529-4242
  • [Journal-full-title] Plastic and reconstructive surgery
  • [ISO-abbreviation] Plast. Reconstr. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] United States
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine
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48. Maronn M, Chamlin S, Metry D: Multifocal tufted angiomas in 2 infants. Arch Dermatol; 2009 Jul;145(7):847-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multifocal tufted angiomas in 2 infants.
  • [MeSH-major] Hemangioma / pathology. Skin Neoplasms / pathology

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  • (PMID = 19620578.001).
  • [ISSN] 1538-3652
  • [Journal-full-title] Archives of dermatology
  • [ISO-abbreviation] Arch Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] United States
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