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Haemangioma

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https://www.readbyqxmd.com/read/29333841/-granular-cell-tumor-of-the-larynx-in-the-child-case-report
#1
Giselle Cuestas, Verónica Rodríguez, Flavia Doormann, Patricio Bellia Munzón, Gastón Bellia Munzón
Laryngeal tumors are uncommon in children, accounting only for 2% of the laryngeal anomalies. Ninety-eight percent are benign; the most frequent ones are recurrent respiratory papillomatosis and haemangioma. Granular cell tumor, also called Abrikossoff tumor, is an unusual benign neoplasm, especially in the larynx. Clinical manifestations depend on the size and location of the tumor. Dysphonia is the main presenting symptom. The diagnosis is confirmed by the biopsy. The treatment of choice is surgery. We present a 9-year-old girl with dysphonia and exertion dyspnea due to a granular cell tumor of the larynx, and we emphasize the importance of considering the endoscopic evaluation of the airway in every child with progressive or persistent dysphonia in order to determine the etiology...
February 1, 2018: Archivos Argentinos de Pediatría
https://www.readbyqxmd.com/read/29331012/capillary-haemangioma-of-lower-lip-in-an-african-patient
#2
Manas Bajpai, Nilesh Pardhe, Manish Kumar
No abstract text is available yet for this article.
October 2017: Journal of Ayub Medical College, Abbottabad: JAMC
https://www.readbyqxmd.com/read/29328009/-a-verrucous-plaque-on-the-lower-leg
#3
F H J Koekelkoren, M Fransen, J C J M Veraart
A 10-year-old boy presented with an asymptomatic, congenital, dark brown coloured, well circumscribed, verrucous, hyperkeratotic plaque on his left leg. This was diagnosed as verrucous haemangioma.
2018: Nederlands Tijdschrift Voor Geneeskunde
https://www.readbyqxmd.com/read/29327066/ramucirumab-induced-multiple-haemangiomas-of-the-skin-two-case-reports
#4
Hideyuki Kosumi, Wataru Nishie, Tatsuro Sugai, Ellen Toyonaga, Norihiro Yoshimoto, Hiroyuki Nakamura, Ryota Horibe, Yasuo Kitamura, Hiroshi Nakatsumi, Hiroshi Shimizu
No abstract text is available yet for this article.
December 20, 2017: Acta Dermato-venereologica
https://www.readbyqxmd.com/read/29183422/congenital-vascular-anomalies-of-the-liver
#5
A Tyraskis, N Durkin, M Davenport
Congenital vascular anomalies of the liver include a range of malformations of the portal venous, hepatic arterial and venous systems. Congenital portosystemic shunts and arteriovenous malformations make up the two most frequent such malformations. While infantile haemangiomas of the liver, endothelial tumours characterised by vascular proliferation should also be considered, as a proportion of them form prenatally. Evidence to support treatment strategies for these infants and children has been mainly based on small case series...
November 6, 2017: South African Medical Journal, Suid-Afrikaanse Tydskrif Vir Geneeskunde
https://www.readbyqxmd.com/read/29134357/apparent-diffusion-coefficient-of-vertebral-haemangiomas-allows-differentiation-from-malignant-focal-deposits-in-whole-body-diffusion-weighted-mri
#6
Jessica M Winfield, Gabriele Poillucci, Matthew D Blackledge, David J Collins, Vallari Shah, Nina Tunariu, Martin F Kaiser, Christina Messiou
OBJECTIVES: The aim of this study was to identify apparent diffusion coefficient (ADC) values for typical haemangiomas in the spine and to compare them with active malignant focal deposits. METHODS: This was a retrospective single-institution study. Whole-body magnetic resonance imaging (MRI) scans of 106 successive patients with active multiple myeloma, metastatic prostate or breast cancer were analysed. ADC values of typical vertebral haemangiomas and malignant focal deposits were recorded...
November 13, 2017: European Radiology
https://www.readbyqxmd.com/read/29131474/photodynamic-therapy-with-double-duration-for-circumscribed-choroidal-haemangioma-functional-and-anatomical-results-based-on-initial-parameters
#7
Daniela Süsskind, Werner Inhoffen, Faik Gelisken, Michael Völker
IMPORTANCE: Pretreatment symptoms longer than twelve months and foveal cystoid changes are indicators for poor anatomical and functional outcome after photodynamic therapy. BACKGROUND: To evaluate the prognostic factors on the effectiveness of photodynamic therapy with double duration for treatment of exudative circumscribed choroidal haemangioma DESIGN: Retrospective study. PARTICIPANTS: Twenty-seven patients with symptomatic exudative circumscribed choroidal haemangioma treated with photodynamic therapy...
November 13, 2017: Clinical & Experimental Ophthalmology
https://www.readbyqxmd.com/read/29118669/glomangiomyoma-of-the-neck-in-a-child-in-nepal-a-rare-case-report-and-literature-review
#8
Bishow Tulachan, Buddha Nath Borgohain
Background: Glomangiomyoma is a rare histological variant of glomus tumour. Clinically, it mimicks as a haemangioma and is challenging to diagnose. Its occurrence in the neck of a child has not been previously described. Case presentation: A 3 year old girl presented with the complaints of painless progressive neck swelling in the right side for one and half year. Sonography, computed tomography (CT), magnetic resonance imaging (MRI), CT neck angiography and fine needle aspiration cytology (FNAC) were suggestive of vacular malformation i...
2017: BMC Ear, Nose, and Throat Disorders
https://www.readbyqxmd.com/read/29111237/imaging-findings-of-primary-hepatic-angiosarcoma-on-gadoxetate-disodium-enhanced-liver-mri-comparison-with-hepatic-haemangiomas-of-similar-size
#9
B Kim, J H Byun, J H Lee, B J Park, H-J Kwon, J H Lee, S J Lee, H J Won, Y M Shin, P N Kim
AIM: To describe imaging characteristics of primary hepatic angiosarcoma on gadoxetate disodium-enhanced dynamic magnetic resonance imaging (MRI) and to determine features that differentiate angiosarcomas from similar-sized haemangiomas. MATERIALS AND METHODS: The study included 15 patients with hepatic angiosarcomas and 35 patients with size-matched hepatic haemangiomas who underwent gadoxetate disodium-enhanced liver MRI. The number, size, growth pattern, signal intensity (SI) characteristics, and SI changes on dynamic scans were evaluated and compared between the two entities...
October 27, 2017: Clinical Radiology
https://www.readbyqxmd.com/read/29103014/giant-calvarial-haemangioma-with-classical-radiological-features
#10
Surya Nandan Prasad, Upendra Chaudhary, Madhuri Kumari, Hira Lal
No abstract text is available yet for this article.
November 4, 2017: BMJ Case Reports
https://www.readbyqxmd.com/read/29102969/hepatic-epithelioid-haemangioendothelioma-hehe-a-diagnostic-dilemma-between-haemangioma-and-angiosarcoma
#11
Belle Vivica van Rosmalen, Joanne Verheij, Saffire S K S Phoa, Thomas Matthijs van Gulik
We present a case of a 77-year-old male patient with a liver tumour diagnosed as hepatic epithelioid haemangioendothelioma (HEHE), a potentially malignant tumour treated with liver resection. The patient is disease-free 3 years after resection. Imaging features using fludeoxyglucose F 18 positron emission tomography CT and MRI with gadoxic acid as well as histopathological findings are discussed.
November 3, 2017: BMJ Case Reports
https://www.readbyqxmd.com/read/29079914/mri-features-of-primary-rare-malignancies-of-the-liver-a-report-from-four-university-centres
#12
Richard C Semelka, Nadesan Nimojan, Saman Chandana, Miguel Ramalho, Suzanne L Palmer, Danielle DeMulder, Carolina Parada Villavicencio, John Woosley, Bonnie L Garon, Reena C Jha, Frank H Miller, Ersan Altun
PURPOSE: To determine if rare primary malignancies of the liver may have consistent features on magnetic resonance imaging (MRI). MATERIALS AND METHODS: This IRB-compliant retrospective study reviewed the records from the pathology departments of four university centres over an 11-year period from 2005-2016 to identify rare primary malignant tumours, which were cross-referenced with MRI records. MRI studies of these patients were reviewed to determine if these tumours exhibited consistent and distinctive features...
October 27, 2017: European Radiology
https://www.readbyqxmd.com/read/29032158/location-affects-the-management-of-liver-haemangioma-a-retrospective-cohort-study
#13
Xiaolei Liu, Zhiying Yang, Haidong Tan, Li Xu, Liguo Liu, Jia Huang, Shuang Si, Yongliang Sun
BACKGROUND: The location of liver haemangioma may affect surgical decisions, but no study has ever examined this issue. METHODS: A retrospective study was performed on 338 liver haemangioma patients who visited at clinic. The collected data included demographics, location, symptoms and whether surgical treatment was performed. For patients with surgical treatment, the collected data included radiologic characteristics, surgical procedures, surgical variables, postoperative stay, morbidity, and mortality...
October 13, 2017: International Journal of Surgery
https://www.readbyqxmd.com/read/29028279/liver-elastography-malignancy-prediction-lemp-score-for-noninvasive-characterization-of-focal-liver-lesions
#14
Ivica Grgurevic, Tomislav Bokun, Nermin N Salkic, Boris Brkljacic, Mirjana Vukelić-Markovic, Tajana Stoos-Veic, Gorana Aralica, Mislav Rakic, Tajana Filipec-Kanizaj, Annalisa Berzigotti
BACKGROUND & AIMS: To analyse elastographic characteristics of focal liver lesions (FLL)s and diagnostic performance of real-time two-dimensional shear-wave elastography (RT-2D-SWE) in order to differentiate benign and malignant FLLs. PATIENTS AND METHODS: Consecutive patients diagnosed with FLL by abdominal ultrasound (US) underwent RT-2D-SWE of FLL and non-infiltrated liver by intercostal approach over the right liver lobe. The nature of FLL was determined by diagnostic work-up, including at least one contrast-enhanced imaging modality (MDCT/MRI), check-up of target organs when metastatic disease was suspected and FLL biopsy in inconclusive cases...
October 13, 2017: Liver International: Official Journal of the International Association for the Study of the Liver
https://www.readbyqxmd.com/read/28969147/pleomorphic-hyalinizing-angiectatic-tumour-a-rare-case-report-and-discussion-of-differential-diagnosis
#15
Ambica Chalmeti, Surekha U Arakeri, Anita P Javalgi, Shefali Goyal
Pleomorphic Hyalinizing Angiectatic Tumour (PHAT) is one of the rare soft tissue tumour which is non-metastasizing. The origin of this tumour is yet uncertain. It occurs in adults as a slow growing subcutaneous mass mimicking clinically and histologically to various benign and malignant soft tissue tumours such as schwannoma, haemangioma and malignant fibrous histiocytoma. The microscopic features of this tumour include clusters of ectatic, fibrin containing, hyalinized blood vessels with pleomorphic and spindle shaped tumour cells showing intranuclear inclusions, stromal haemosiderin pigment and a variable inflammatory infiltrate...
August 2017: Journal of Clinical and Diagnostic Research: JCDR
https://www.readbyqxmd.com/read/28954747/primary-cutaneous-ewing-sarcoma-presenting-as-a-chest-wall-lesion
#16
Jie Hua Xu, Vindya Abeysinghe, Anne Louise Ryan, Kishore Sieunarine
A 10-year-old boy presents with a rare case of primary cutaneous Ewing sarcoma. The left-sided chest wall lesion was initially thought to be a benign haemangioma and treated with cryotherapy. Within 4 months, the lesion returned and post excision was found to be primary cutaneous Ewing sarcoma on histology. Few cases of primary cutaneous Ewing sarcoma exist in the literature, and although it is a rare differential for paediatric skin lesions, it is an important consideration due to the associated mortality risk in this young cohort...
September 27, 2017: BMJ Case Reports
https://www.readbyqxmd.com/read/28942665/-infantile-haemangioma-clinical-and-demographic-characteristics-experiences-in-the-treatment
#17
Zsanett Renáta Csoma, Szandra Dalmády, Rita Ábrahám, Tamás Rózsa, Katalin Rácz, Lajos Kemény
INTRODUCTION: Infantile haemangiomas are the most common vascular tumours of infancy. The vast majority of the lesions do not require dermatological treatment due to their unique clinical course and the high rate of spontaneous regression. Approximately 10-15% of the tumours result in severe complications and sequale, requiring special management and close follow-up. AIM: The aim of the present study was to assess the data of the patients treated with infantile haemangiomas, and to summarize the results of the therapy during 4...
October 2017: Orvosi Hetilap
https://www.readbyqxmd.com/read/28927653/patient-age-affects-the-growth-of-liver-haemangioma
#18
Xiaolei Liu, Zhiying Yang, Haidong Tan, Li Xu, Liguo Liu, Jia Huang, Shuang Si, Yongliang Sun, Wenying Zhou
BACKGROUND: The aim of this study was to report the prevalence of liver haemangioma and describe growth rates by age. METHODS: A retrospective study of people undergoing a health examination. The collected data included gender, age, presence or absence and size of liver haemangioma. A second database of liver haemangioma patients with a minimum follow up period of 5 years was analysed. The collected data included gender, initial age at diagnosis, follow-up period, initial and final size...
September 16, 2017: HPB: the Official Journal of the International Hepato Pancreato Biliary Association
https://www.readbyqxmd.com/read/28899875/stridor-is-not-always-croup-infantile-haemangioma-in-the-airway
#19
Joana Cunha Oliveira, Inês Azevedo, Augusta Gonçalves, Carla Moreira
No abstract text is available yet for this article.
September 12, 2017: BMJ Case Reports
https://www.readbyqxmd.com/read/28893050/-quirky-bulb-on-the-lower-jaw-an-organizing-haematoma
#20
Raghavendra Mahadev Naik, Ramanjaneya Raju Pennemetsa, Sudhakara Reddy, Praveen Gadde, Sruthi Rayapureddy
Organizing Haematoma is a rare, non/neoplastic benign lesion with locally destructive behaviour that may mimic a malignancy. Usually symptoms do not occur, while the lesion remains localized. An Organized Haematoma is an encapsulated blood clot undergoing neovascularization and fibrosis. It has also been referred to as a hemophilic pseudotumour and/or a haematoma like tumour, which is rarely found in the head and neck region. Other reported cases have been related to trauma or an underlying haemangioma. However, most of the cases have no identifiable underlying pathology, trauma or systemic disease...
July 2017: Journal of Clinical and Diagnostic Research: JCDR
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