Lobular Capillary Hemangioma of the External Jugular Vein: A Rare Case Report (original) (raw)
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Lobular Capillary Hemangioma of Head and Neck Region: A Retrospective Study in A Tertiary Centre
Scholarly journal of otolaryngology, 2020
Lobular capillary hemangioma (LCH) is synonymously known as pyogenic granuloma, epulis gravidarum, eruptive hemangioma, granulation tissue-type hemangioma, granuloma gravidarum, pregnancy tumor and botryomycome [1-3]. It is a benign, fast growing, capillary proliferation with a microscopically distinct lobular architecture that affects the skin and mucous membranes of the oral and, rarely, of the nasal cavities and internal organs such as brain and liver [4-9]. Poncet and Dor were the first ones to describe it in 1897 as human botryomycosis and referred to these tumors as small vascular tumors in the fingers of four patients [1,7,10,11]. Oral cavity mucosa is the predominant site for LCH occurrence, but nasal cavity involvement is rare. Anterior septum (Little's area) is the most frequently affected site followed by turbinate, but lesions have also been described arising from the maxillary sinus, roof of nasal cavity and floor of nasal vestibule
Intraoral Capillary Hemangioma as a Benign Tumor: A Rare Case Report
Journal of Oral Health and Community Dentistry
Introduction: Hemangioma is a relatively common benign proliferation of blood vessels that primarily develops during childhood and rarely in adult patients. Two main forms of hemangioma are recognized as capillary and cavernous. The capillary form presents as a flat area consisting of numerous small capillaries. Cavernous hemangioma appears as an elevated lesion of a deep red color and consists of large dilated sinuses filled with blood. The aim of the study was to report the case of an intraoral capillary hemangioma in a patient and to describe the successful treatment of this case. Case presentation: The patient was a 54-year-old male who presented to the
Internal Jugular Vein Hemangioma
Annals of Vascular Surgery, 2012
Primary tumors of the major body veins arising intraluminally are rare clinical entities. As such, few cases have been reported in the literature. As a primary tumor, hemangiomas arising in the internal jugular vein are extremely rare, while those arising in the external jugular vein are only slightly more common. We present a case of an internal jugular vein hemangioma that was incidentally discovered during an ultrasound examination performed for the evaluation of the internal carotid arteries. We believe that this is the second case of internal jugular vein hemangioma reported in the English literature.
A Rare Case of Intraosseous Papillary Hemangioma of the Head and Neck
Objectives Papillary hemangioma (PH) is a novel variant of intravascular capillary hemangioma. It is more common in adults and has a male predominance. Most tumors reported so far are solitary and cutaneous. Here we present a rare case of an intraosseous PH involving the frontal bone. Methods Brain imaging in a 69-year-old male with a slowly enlarging swelling on the right frontal area following an accidental fall demonstrated a 4.5 cm x 1.7 cm x 4.2 cm mass originating from the right frontal bone, with a tiny defect on the orbital roof. A malignant process was favored, and the mass was removed. Results Histopathology revealed a vascular lesion showing intraosseous distribution with foci of extension into the fibrous connective tissue. There were areas of plump endothelial cells with intracytoplasmic hyaline globules arranged in papillary configuration. The lesional cells were immunoreactive with CD34 and vimentin. AE1/AE3, EMA, PR, D2-40, inhibin and S100 stains were negative. Ki-6...
Intranasal lobular capillary hemangioma: A series of five cases
Respiratory Medicine Case Reports, 2020
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Intraosseous Hemangioma: A Case Report and Review of Literature
International Journal of Head and Neck Surgery, 2013
Intraosseous vascular lesions are rare conditions, comprising only 0.5 to 1% of all intraosseous hemangioma tumors. They mainly occur in the second decade of life especially in female. The most common locations are the vertebral column and skull; nevertheless, the mandible is quite rare location. Hemangiomas are benign vasoformative neoplasms of endothelial origin. However, the origin of central hemangioma is debatable. Cavernous hemangioma produces dilemma in diagnosis with central gaint cell tumor, aneurysmal bone cyst, ameloblastoma, cystic lesion such as residual cyst, keratocyst and fibro-osseous lesions, such as fibrous dysplasia being frontier in clinical diagnosis. Here, we report a 6 years male with cavernous hemangioma of mandible.
Lobular Capillary Hemangioma at an Unusual Location: A Rare Occurrence
A female patient aged 50 years presented with difficulty in swallowing and foreign body sensation in the throat for 2 months. She had no history of previous neck surgery or intubation. There was no history of odynophagia or change of voice. The patient had no history of weight loss or loss of appetite. Video laryngoscopy showed an exophytic pinkish, globular, pedunculated fleshy mass in the left pyriform sinus reaching the posterior pharyngeal wall (Fig. 1). Bilateral vocal cords were normal and mobile. Contrast-enhanced computer tomography (CECT) of the neck showed a well-defined avidly enhancing pedunculated mass of 1.5 x 1.6 cm arising from the left pyriform sinus on the axial view (Fig. 2). The patient underwent micro laryngoscopic excision of the mass (Fig. 3). Cystic vascular growth was seen arising from the left pyriform sinus.
Lobular capillary hemangioma: A case report
International Journal of Medical and Dental Case Reports
Lobular capillary hemangioma also known as pyogenic granuloma is a rapidly growing benign neoplasm of oral cavity and mucous membrane. The present case is about a 65-year-old male patient who had reported with a chief complaint of pain in the right posterior back tooth region since 2-3. Lobular capillary hemangioma is normally presented on the gingiva as a response local irritation such as calculus, fractured tooth, minor trauma, rough dental restorations, and foreign materials. Here, in this case, we excised the lesion and the histopathological report confirms the diagnosis.
Intracranial capillary hemangioma: case report and review of the literature
Surgical Neurology, 2005
Background: Capillary hemangiomas are benign vascular lesions that commonly present at birth or in early infancy on the face, scalp, back, or chest. The authors present an exceedingly rare case of an intracranial capillary hemangioma arising in an adult. Only 4 biopsy-proven cases have been reported in the pediatric population previous to this case report. Case Description: A 31-year-old pregnant woman presented at 38 weeks of gestation with severe headaches, nausea, and vomiting. Imaging revealed an extra-axial mass lesion arising from the tentorium with both supra-and infratentorial components. The patient underwent a resection of her tumor, which was diagnosed as a capillary hemangioma by histopathologic examination. The patient required 2 further resections after the lesion exhibited a rapid regrowth from residual tumor in the left transverse sinus. The patient has remained free of disease 41 months out from her third surgery. Conclusions: Intracranial capillary hemangiomas are exceedingly rare entities, with a capability for rapid growth. When gross total resection cannot be achieved, these patients should be observed closely, and the use of adjuvant radiotherapy should be considered. D