Kaposiform Hemangioendothelioma of the Oral Cavity: A Rare Tumor with an Unusual Location

被引：2

作者：

Morais, Thayna M. de Lima ^{[1
]}

Sanchez-Romero, Celeste ^{[2
]}

Ribeiro, Luciano ^{[3
]}

Fae, Daniele S. ^{[4
]}

Verner, Francielle S. ^{[4
]}

de Almeida, Oslei P. ^{[1
]}

de Aquino, Sibele Nascimento ^{[4
]}

机构：

[1] Univ Estadual Campinas, Oral Pathol, Dept Oral Diag, Piracicaba Dent Sch, Piracicaba, Brazil

[2] Univ Republica, Mol Pathol Area, Fac Dent, Montevideo, Uruguay

[3] Brazilian Assoc Dent, Governador Valadares, MG, Brazil

[4] Univ Fed Juiz de Fora, Dept Dent, Oral Diag, Governador Valadares, Brazil

来源：

HEAD & NECK PATHOLOGY | 2021年 / 15卷 / 04期

关键词：

Hemangioendothelioma; Kaposiform Hemangioendothelioma; Head and neck neoplasms; Vascular neoplasms; Kasabach− Merritt syndrome; Oral diagnosis;

D O I：

10.1007/s12105-021-01316-6

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

Kaposiform hemangioendothelioma is a rare neoplasm with intermediate malignant behavior, mainly affecting infants and children. Involvement head and neck is uncommon, and there are only four cases reported in the oral cavity and oropharynx. Microscopically, it is characterized by a vascular proliferation permeated by spindle-to-ovoid cells resembling Kaposi sarcoma. Immunohistochemically, the tumor is positive for CD31, CD34 and negative for D2-40. Herein we present a rare case of intraoral Kaposiform hemangioendothelioma in a 10-year-old boy.

引用

页码：1421 / 1425

页数：5

共 36 条

[1] Kaposiform Hemangioendothelioma of the Oral Cavity: A Rare Tumor with an Unusual Location
Thayná M. de Lima Morais
Celeste Sánchez-Romero
Luciano Ribeiro
Daniele S. Faé
Francielle S. Verner
Oslei P. de Almeida
Sibele Nascimento de Aquino
Head and Neck Pathology, 2021, 15 : 1421 - 1425
[2] Kaposiform Hemangioendothelioma: clinicopathological characteristics of 8 cases of a rare vascular tumor and review of literature
Qurratulain Chundriger
Muhammad Usman Tariq
Jamshid Abdul-Ghafar
Arsalan Ahmed
Nasir Ud Din
Diagnostic Pathology, 16
[3] Kaposiform Hemangioendothelioma: clinicopathological characteristics of 8 cases of a rare vascular tumor and review of literature
Chundriger, Qurratulain
Tariq, Muhammad Usman
Abdul-Ghafar, Jamshid
Ahmed, Arsalan
Din, Nasir Ud
DIAGNOSTIC PATHOLOGY, 2021, 16 (01)
[4] Report Intramuscular composite hemangioendothelioma: case report of an unusual tumor in an unusual location
Chin, Susie
Kim, Jiyoon
Jung, Min
Kim, Min Ju
Moon, Ahrim
Kim, Hee Kyung
Kim, Young Hwan
Koh, Eun Suk
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2020, 13 (06): : 1421 - 1425
[5] Kaposiform hemangioendothelioma in an unusual site: A report of two cases in children
Bhattacharya, Sumanta
Roy, Paromita
Chatterjee, Uttara
Bhattacharyya, Arpita
INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY, 2022, 65 (01) : 167 - 169
[6] Surgical treatment of kaposiform hemangioendothelioma in the pelvic cavity, bladder and ureter
Xiao, Li
Dong, Changxian
Zuo, Song
Wang, Yanlin
JOURNAL OF PEDIATRIC SURGERY CASE REPORTS, 2018, 28 : 72 - 76
[7] Pseudomyogenic Hemangioendothelioma: A Vascular Tumor Previously Undescribed in the Oral Cavity
Rawal Y.B.
Anderson K.M.
Dodson T.B.
Head and Neck Pathology, 2017, 11 (4) : 525 - 530
[8] Microscopic Kaposiform Hemangioendothelioma With Extensive Lymphangiomatosis: An Extraordinary Example of an Unusual Entity
Low, Irene C.
Yang, Rita Y. -T.
Symmans, Pennie J.
INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2013, 21 (03) : 297 - 302
[9] Kaposiform hemangioendothelioma in children: a benign vascular tumor with multiple treatment options
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Klenk, Anne K.
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WORLD JOURNAL OF PEDIATRICS, 2018, 14 (04) : 322 - 329
[10] Intracranial kaposiform hemangioendothelioma presenting as epistaxis: a rare case report with review of literature
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Harsh Deora
Shilpa Rao
Sandeep Kandregula
Suma Mysore Narayana
Child's Nervous System, 2021, 37 : 2057 - 2062

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