Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease

Abstract Background Epithelioid hemangioendothelioma (EHE) is an especially rare, low-grade malignant vascular tumor that, according to WHO classification, is described as locally aggressive tumor with possible metastasis and makes up 1% of all vascular tumors. EHE is characterized by the accumulati...

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Main Authors: Gintaras Januzis, Dovydas Sakalys, Martynas Mantas Krukis, Dmitrij Seinin
Format: Article
Language:English
Published: BMC 2020-11-01
Series:BMC Oral Health
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12903-020-01291-4
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spelling doaj-cb88a3a9e5d84294980b7cc7c85a135f2020-11-25T04:08:53ZengBMCBMC Oral Health1472-68312020-11-012011710.1186/s12903-020-01291-4Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal diseaseGintaras Januzis0Dovydas Sakalys1Martynas Mantas Krukis2Dmitrij Seinin3Department of Maxillofacial Surgery, Faculty of Odontology, Lithuanian University of Health SciencesDepartment of Maxillofacial Surgery, Faculty of Odontology, Lithuanian University of Health SciencesDepartment of Maxillofacial Surgery, Faculty of Odontology, Lithuanian University of Health SciencesNational Center of Pathology, Vilnius University Hospital Santaros ClinicsAbstract Background Epithelioid hemangioendothelioma (EHE) is an especially rare, low-grade malignant vascular tumor that, according to WHO classification, is described as locally aggressive tumor with possible metastasis and makes up 1% of all vascular tumors. EHE is characterized by the accumulation of round, eosinophil-infiltrated endothelium cells; with vacuolation of their cytoplasm; frequent angiocentric inflammation; and myxohyaline stroma. This tumor is usually found in the liver, lungs, and bones and is especially rare in the mouth. Case presentation We present an 18-year-old Caucasian female whose oral cavity lesion had been misdiagnosed as marginal periodontitis. The patient was treated improperly for 2 years until she was referred to a maxillofacial surgeon. The patient complained only about gingival recession in the palatal area of her upper-right-side 13th, 14th, and 15th teeth. The lesion’s clinical appearance was of locally ulcerated painless lesion that affect the underlying bone as seen in X-rays in the palatal side of the right canine and the first and second premolars. Patient underwent surgery for her present defect and reconstruction using allogenic bone transplant. The diagnosis of EHE was based on the bony destruction as seen in x-rays and in the accumulation of tumor cells that were 100% positive to CD31; CD34 and ERG to endothelial markers. During the 31-month follow-up period, the patient exhibited no clinical and radiographic complications. Conclusions With this clinical case, we demonstrate that this rare tumor must be included in differential diagnoses of periodontal pathologies to perform histomorphological examination in a timely manner, which could lead to correct diagnosis and adequate treatment.http://link.springer.com/article/10.1186/s12903-020-01291-4Epithelioid hemangioendotheliomaOral cancerVascular tumorEndothelial cellsPeriodontitisGingival pathologies
collection DOAJ
language English
format Article
sources DOAJ
author Gintaras Januzis
Dovydas Sakalys
Martynas Mantas Krukis
Dmitrij Seinin
spellingShingle Gintaras Januzis
Dovydas Sakalys
Martynas Mantas Krukis
Dmitrij Seinin
Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease
BMC Oral Health
Epithelioid hemangioendothelioma
Oral cancer
Vascular tumor
Endothelial cells
Periodontitis
Gingival pathologies
author_facet Gintaras Januzis
Dovydas Sakalys
Martynas Mantas Krukis
Dmitrij Seinin
author_sort Gintaras Januzis
title Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease
title_short Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease
title_full Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease
title_fullStr Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease
title_full_unstemmed Maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease
title_sort maxillary epithelioid hemangioendothelioma: an especially rare malignant tumor mimicking periodontal disease
publisher BMC
series BMC Oral Health
issn 1472-6831
publishDate 2020-11-01
description Abstract Background Epithelioid hemangioendothelioma (EHE) is an especially rare, low-grade malignant vascular tumor that, according to WHO classification, is described as locally aggressive tumor with possible metastasis and makes up 1% of all vascular tumors. EHE is characterized by the accumulation of round, eosinophil-infiltrated endothelium cells; with vacuolation of their cytoplasm; frequent angiocentric inflammation; and myxohyaline stroma. This tumor is usually found in the liver, lungs, and bones and is especially rare in the mouth. Case presentation We present an 18-year-old Caucasian female whose oral cavity lesion had been misdiagnosed as marginal periodontitis. The patient was treated improperly for 2 years until she was referred to a maxillofacial surgeon. The patient complained only about gingival recession in the palatal area of her upper-right-side 13th, 14th, and 15th teeth. The lesion’s clinical appearance was of locally ulcerated painless lesion that affect the underlying bone as seen in X-rays in the palatal side of the right canine and the first and second premolars. Patient underwent surgery for her present defect and reconstruction using allogenic bone transplant. The diagnosis of EHE was based on the bony destruction as seen in x-rays and in the accumulation of tumor cells that were 100% positive to CD31; CD34 and ERG to endothelial markers. During the 31-month follow-up period, the patient exhibited no clinical and radiographic complications. Conclusions With this clinical case, we demonstrate that this rare tumor must be included in differential diagnoses of periodontal pathologies to perform histomorphological examination in a timely manner, which could lead to correct diagnosis and adequate treatment.
topic Epithelioid hemangioendothelioma
Oral cancer
Vascular tumor
Endothelial cells
Periodontitis
Gingival pathologies
url http://link.springer.com/article/10.1186/s12903-020-01291-4
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