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Haemangioma

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https://www.readbyqxmd.com/read/28438388/kaposiform-haemangioendothelioma-a-review-with-emphasis-on-histological-differential-diagnosis
#1
REVIEW
Juan Putra, Anita Gupta
Kaposiform haemangioendothelioma (KHE) is a rare, locally aggressive/borderline vascular tumour primarily seen in neonates and children. KHE is occasionally associated with Kasabach-Merritt phenomenon and tends to have a poor clinical prognosis. While the histological features of tufted angiomas and KHE overlap, some believe tufted angiomas are a milder, benign, more localised counterpart of KHE. The other histological differential diagnoses of KHE include infantile haemangioma, congenital haemangioma, spindle cell haemangioma, verrucous malformation/haemangioma, and Kaposi sarcoma...
April 21, 2017: Pathology
https://www.readbyqxmd.com/read/28435577/intra-articular-localized-haemangioma-of-the-knee-mimicking-localized-pigmented-villonodular-synovitis-a-case-report
#2
G K Goki-Kamei, N M Norimasa-Matsubara, T T Teruyasu-Tanaka, K N Koji-Natsu, T S Toshihiro-Sugioka
Intra-articular synovial haemangioma of the knee is a benign tumour. However, diagnostic delay leads to degenerative changes in the cartilage and osteoarthritis due to recurrent haemarthrosis. Therefore, treatment should be performed immediately. We report the case of a localized synovial haemangioma arising from the medial plica in a 38-year old female presenting with pain and restricted range of motion in the right knee joint. Initially, we diagnosed this case as a localized pigmented villonodular synovitis (LPVS) based on MRI and arthroscopic findings and performed only arthroscopic en bloc excision of the mass and synovectomy around the mass for diagnostic confirmation...
March 2017: Malaysian Orthopaedic Journal
https://www.readbyqxmd.com/read/28409039/endodontic-management-of-teeth-juxtaposed-to-haemangioma
#3
Rekha Chandra Mani, Anchu Rachel Thomas, Premkumar Elavarasu, Vijay Venkatesh
Vascular anomalies are localized defects in the vasculature that may or may not be present at birth. There are many types of vascular anomalies with different aetiology and clinical picture and, therefore, require the combined expertise of medical, radiological, and surgical specialities for its diagnosis and management. The term "haemangioma" is used as a common generic label to incorporate all types of vascular malformations. In this report, we describe a case of two maxillary premolars, requiring endodontic therapy, in close proximity to a haemangioma...
2017: Case Reports in Dentistry
https://www.readbyqxmd.com/read/28399783/fu-j-liu-z-chen-x-acral-necrosis-induced-by-sodium-morrhuate-sclerotherapy-in-infantile-haemangioma-a-case-report-j-hand-surg-eur-2017-42-206-7
#4
C J Deutsch, G S Pahal, D Nikkhah
No abstract text is available yet for this article.
May 2017: Journal of Hand Surgery, European Volume
https://www.readbyqxmd.com/read/28397661/-medical-treatment-of-children-with-infantile-haemangiomas
#5
Hanne Kalleklev Velure, Ulla Birgitte Hartling, Anette Schuster, Annette Bygum
Infantile haemangioma is a benign vascular tumour seen in 4-5% of infants. It has a characteristic life cycle comprised by a proliferative phase and a spontaneous involution phase. Most infantile haemangiomas do not require intervention. Treatment is relevant when there is a risk of functional impairment or cosmetic disfigurement, or if the haemangiomas are painful and ulcerating. The beta blocker propranolol has been shown to be an excellent first-line treatment, and we present an algorithm for therapeutic decision and monitoring...
February 20, 2017: Ugeskrift for Laeger
https://www.readbyqxmd.com/read/28393045/treatment-of-diffuse-choroidal-haemangioma-using-photodynamic-therapy
#6
Khay Wei Poh, Yong Zheng Wai, Jamalia Rahmat, Manoharan Shunmugam, Joseph Alagaratnam, Sunder Ramasamy
No abstract text is available yet for this article.
2017: International Journal of Ophthalmology
https://www.readbyqxmd.com/read/28389894/upper-fornix-approach-combined-with-a-superior-lateral-cantholysis-a-minimally-invasive-approach-to-the-superonasal-intraconal-space
#7
Ho-Seok Sa, Ji Won Seo, Sunah Kang
PURPOSE: To present a new minimally invasive approach to the deep superonasal orbit. METHODS: This retrospective study reviewed seven consecutive patients who underwent orbital surgery using an upper conjunctival fornix approach combined with a superior lateral cantholysis for tumors in the superonasal intraconal space. Charts were reviewed for demographic, radiological, clinical, and surgical data including surgical outcome and morbidities for each patient. RESULTS: Six benign tumors of the superonasal intraconal orbit were successfully exposed and removed using this approach, and one malignant tumor was biopsied for diagnosis...
April 7, 2017: Japanese Journal of Ophthalmology
https://www.readbyqxmd.com/read/28388343/orbital-melanoma-masquerading-as-a-galloping-haemangioma
#8
Daniele Lorenzano, Katherine Miszkiel, Geoffrey E Rose
We describe a 32-year-old pregnant woman who was referred to our clinic after 6 weeks of observation elsewhere with a rapidly expanding orbital mass, proptosed globe and slowly decreasing of vision in her left eye. To our examination the patient presented with congested optic disc fine macular striae and some slight choroidal elevation without any retinal pigmentation. An MRI scan without contrast was performed, suggesting the signal charactheristics of an orbital mass consistent with a cellular lesion such as a cavernous hemangioma or a solitary fibrous tumour...
April 2017: Orbit
https://www.readbyqxmd.com/read/28385254/-infantile-haemangioma-protein-g-implicated-once-more
#9
O Dereure
No abstract text is available yet for this article.
April 3, 2017: Annales de Dermatologie et de Vénéréologie
https://www.readbyqxmd.com/read/28384953/neonatal-airway-compromise-by-a-giant-cervicothoracic-venous-haemangioma
#10
Janardhan Shenoy, Anita Coutinho, Sowmini P Kamath, Suresh Pai, Santosh Pv Rai
Haemangiomas are most common non-malignant vascular tumours of infancy. Here, we describe an antenatally detected mass over the neck causing compressive respiratory compromise at birth requiring resuscitative measures at birth. The mass showed increased vascularity on Contrast Enhanced Computed Tomography (CECT) with extension upto superior mediastinum. Surgical excision was required following failure to medical measures with steroids and propranolol. Histopathology confirmed it to be a venous haemangioma. This case highlights that these benign lesions may reach large sizes and antenatal detection may help in planning effective delivery and resuscitative measures...
February 2017: Journal of Clinical and Diagnostic Research: JCDR
https://www.readbyqxmd.com/read/28384897/intramuscular-capillary-haemangioma-of-the-temporalis-muscle-a-rare-case-with-a-review-of-the-literature
#11
Nikhil Arora, Eishaan Kamta Bhargava, Arif Kavungal Nambillath, Ravi Meher
An Intramuscular Haemangioma (IMH) is a benign mesenchymal tumour of the endothelial cells that accounts for less than 1% of all haemangiomas. Here we report the case of a capillary type intramuscular haemangioma in a five-year-old boy, only the fourth such case reported in literature, along with a relevant review of the literature. The lesion was surgically managed, with no recurrence in the follow up period till date.
February 2017: Journal of Clinical and Diagnostic Research: JCDR
https://www.readbyqxmd.com/read/28348632/primary-ocular-adnexal-extranodal-marginal-zone-mucosa-associated-lymphoid-tissue-malt-lymphoma-presenting-as-orbital-apex-syndrome
#12
Carlen A Yuen, John H Pula, Milap Mehta
A 75-year-old female with a past medical history significant for prior stroke and atrial fibrillation presented with acute onset of orbital apex syndrome with chemosis and periorbital ecchymosis. Following initial treatment to relieve intraocular pressure, she began spontaneously haemorrhaging retro-orbitally. Preliminary investigation with neuroimaging demonstrated a left orbital mass with extension into the orbital apex. A provisional diagnosis of cavernous haemangioma was made. She was treated with transorbital resection of the orbital mass...
April 2017: Neuro-ophthalmology
https://www.readbyqxmd.com/read/28336941/analysis-of-factors-affecting-the-therapeutic-effect-of-propranolol-for-infantile-haemangioma-of-the-head-and-neck
#13
Jian-Yong Dong, Jie-Xin Ning, Kai Li, Chao Liu, Xu-Xia Wang, Rong-Hui Li, Lin-Lin Yue, Ying-Ying Huang, Shao-Hua Liu
Infantile haemangiomas (IHs) are the most common congenital vascular tumours of infancy. Propranolol has been demonstrated to be effective for IHs; however, the factors affecting its therapeutic effect remain unknown. We enrolled 169 infants with IHs of the head and neck region treated with oral propranolol at a dose of 2.0 mg/kg/day. We evaluated the therapeutic responses 6 months after treatment and the end of treatment, which were categorized into four grades. The type and location of the lesions and the infant age at treatment initiation were analysed...
March 23, 2017: Scientific Reports
https://www.readbyqxmd.com/read/28330684/mri-for-the-detection-of-calcific-features-of-vertebral-haemangioma
#14
Y Y Bender, S M Böker, G Diederichs, T Walter, M Wagner, E Fallenberg, T Liebig, M Rickert, B Hamm, M R Makowski
AIM: To evaluate the diagnostic performance of susceptibility-weighted-magnetic-resonance imaging (SW-MRI) for the detection of vertebral haemangiomas (VHs) compared to T1/T2-weighted MRI sequences, radiographs, and computed tomography (CT). MATERIALS AND METHODS: The study was approved by the local ethics review board. An SW-MRI sequence was added to the clinical spine imaging protocol. The image-based diagnosis of 56 VHs in 46 patients was established using T1/T2 MRI in combination with radiography/CT as the reference standard...
March 19, 2017: Clinical Radiology
https://www.readbyqxmd.com/read/28262494/-18-f-florbetapir-uptake-in-a-primary-intraosseous-haemangioma-displayed-in-a-cerebral-pet-ct
#15
R Sánchez-Vañó, S Prado-Wohlwend, P Sopena-Novales, E Uruburu-García, M D Monedero-Picazo, C Martínez-Carsí
No abstract text is available yet for this article.
March 2, 2017: Revista Española de Medicina Nuclear e Imagen Molecular
https://www.readbyqxmd.com/read/28251817/wound-management-of-ulcerated-haemangioma-of-infancy%C3%A2-%C3%A2-an-audit
#16
Zerina Lokmic, Taya Grainger, Nadeeja V Atapattu, Roderic J Phillips, Anthony J Penington
Haemangioma of infancy, a benign tumour of blood vessels, is the most common tumour of infancy. Ulceration, the most common complication, presents a unique wound care challenge. A retrospective audit of medical records of children with haemangioma of infancy who presented to the Royal Children's Hospital, Melbourne, Australia, between January 2000 and December 2014 was undertaken with an aim to examine wound management of ulcerated haemangioma of infancy. In total, 535 hospital medical records were identified as suitable, of which 352 were randomly selected and audited, of which 84 patients had ulcerated haemangioma of infancy, and 62 were subject to wound management...
March 1, 2017: International Wound Journal
https://www.readbyqxmd.com/read/28251611/consensus-statement-for-the-treatment-of-infantile-haemangiomas-with-propranolol
#17
Sarah L Smithson, Marius Rademaker, Susan Adams, Stuart Bade, Philip Bekhor, Samantha Davidson, Amanda Dore, Catherine Drummond, Gayle Fischer, Alexander Gin, Claire Grills, Anne Halbert, Zerina Lokmic, Emma McCahon, Vanessa A Morgan, Dedee F Murrell, David Orchard, Anthony Penington, Diana Purvis, John Relic, Susan Robertson, Aaron J Robinson, Laura Scardamaglia, John Su, Swee Tan, Orli Wargon, Lachlan Warren, Li-Chuen Wong, Tania Zappala, Roderic Phillips
Although most infantile haemangiomas do not require treatment due to a natural history of spontaneous involution, some require early intervention. The Australasian Vascular Anomalies Network and the Australasian Paediatric Dermatology Network have developed a consensus statement for the treatment of infantile haemangiomas with oral propranolol. Infants with haemangiomas that are life threatening, at risk of ulceration, or at risk of causing a significant functional impairment, psychological impact or physical deformity should be treated early with oral propranolol...
March 1, 2017: Australasian Journal of Dermatology
https://www.readbyqxmd.com/read/28247230/update-from-the-4th-edition-of-the-world-health-organization-of-head-and-neck-tumours-tumours-of-the-oral-cavity-and-mobile-tongue
#18
Susan Müller
There have been several additions and deletions in Chapter 4 on Tumours of the oral cavity and mobile tongue in the 2017 fourth edition of the World Health Organization Classification of Tumours of the Head and Neck. This chapter excludes the oropharynx, which now is a stand-alone chapter acknowledging the uniqueness of the oropharynx from the oral cavity. New entries in Chapter 4 include rhabdomyoma, haemangioma, schwannoma, neurofibroma and myofibroblastic sarcoma in the section titled Soft tissue and neural tumours...
March 2017: Head and Neck Pathology
https://www.readbyqxmd.com/read/28238417/enhanced-expression-of-programmed-cell-death-1-pd-1-protein-in-benign-vascular-anomalies
#19
Clarissa N Amaya, Frank H Wians, Brad A Bryan, Alireza Torabi
Programmed cell death 1 (PD-1) and its ligands have been shown to play a significant role in evasion of malignant tumour cells from the immune system. Last year, the United States Food and Drug Administration (FDA) approved anti-PD-1 inhibitors for treatment of non-small cell lung carcinoma and recently has approved anti-PD-L1 blocker for treatment of metastatic urothelial cell carcinoma. However, the role that the immune system might have on benign tumours including vascular anomalies has received less attention...
April 2017: Pathology
https://www.readbyqxmd.com/read/28224302/retinal-cavernous-haemangioma-treated-by-proton-beam-therapy
#20
Amir Mahdjoubi, Rémi Dendale, Livia Lumbroso-Le Rouic, Laurence Desjardins, Nathalie Cassoux
As one of intraocular tumours, retinal cavernous haemangioma is a benign vascular lesion that is mostly unilateral. Very few cases about cavernous haemangioma treatment are reported, and there is currently no consensus on the most effective treatment. This clinical case reports on a 40-year-old male, presenting a peripheral retinal cavernous haemangioma, complicated with a repetitive vitreous haemorrhage causing bad vision. Several therapeutic methods were unsuccessfully attempted to stop haemorrhagic recurrences...
February 21, 2017: International Ophthalmology
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