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Hemangioma

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1. Haemangioma

months; 80% of growth typically occurs by the end of the fourth month. Thereafter involution takes place at an approximate rate of 10% per year so that, by age 5 years, 50% of haemangiomas have completed involution. Complete resolution is possible, but in many cases cutaneous stigmata remain, with redundant fibro-fatty tissue and telangiectasias. Garzon MC. Infantile hemangioma. In: Callen JP, Horn TD, Mancini AJ, et al, eds. Dermatology. Vol. 2. 2nd ed. St. Louis, MO: Elsevier; 2008:1565-80. Finn MC (...) , Glowacki J, Mulliken JB. Congenital vascular lesions: clinical application of a new classification. J Pediatric Surg. 1983 Dec;18(6):894-900. http://www.ncbi.nlm.nih.gov/pubmed/6663421?tool=bestpractice.com Chang LC, Haggstrom AN, Drolet BA, et al. Growth characteristics of infantile hemangiomas: implications for management. Pediatrics. 2008 Aug;122(2):360-7. http://www.ncbi.nlm.nih.gov/pubmed/18676554?tool=bestpractice.com Congenital haemangiomas are distinct from infantile haemangiomas

2018 BMJ Best Practice

2. Interventions for infantile haemangiomas of the skin. Full Text available with Trip Pro

Interventions for infantile haemangiomas of the skin. Infantile haemangiomas (previously known as strawberry birthmarks) are soft, raised swellings of the skin that occur in 3% to 10% of infants. These benign vascular tumours are usually uncomplicated and tend to regress spontaneously. However, when haemangiomas occur in high-risk areas, such as near the eyes, throat, or nose, impairing their function, or when complications develop, intervention may be necessary. This is an update of a Cochrane (...) Review first published in 2011.To assess the effects of interventions for the management of infantile haemangiomas in children.We updated our searches of the following databases to February 2017: the Cochrane Skin Group Specialised Register, CENTRAL, MEDLINE, Embase, PsycINFO, AMED, LILACS, and CINAHL. We also searched five trials registries and checked the reference lists of included studies for further references to relevant trials.Randomised controlled trials (RCTs) of all types of interventions

2018 Cochrane

6. Clinical Practice Guideline for the Management of Infantile Hemangiomas

Clinical Practice Guideline for the Management of Infantile Hemangiomas Clinical Practice Guideline for the Management of Infantile Hemangiomas | From the American Academy of Pediatrics | Pediatrics '); document.write(''); } function OAS_AD(pos) { if (OAS_version >= 11 && typeof(OAS_RICH)!='undefined') { OAS_RICH(pos); } else { OAS_NORMAL(pos); } } //--> Search for this keyword Source User menu Sections Sign up for highlighting editor-chosen studies with the greatest impact on clinical care (...) . Clinical Practice Guideline for the Management of Infantile Hemangiomas Daniel P. Krowchuk , Ilona J. Frieden , Anthony J. Mancini , David H. Darrow , Francine Blei , Arin K. Greene , Aparna Annam , Cynthia N. Baker , Peter C. Frommelt , Amy Hodak , Brian M. Pate , Janice L. Pelletier , Deborah Sandrock , Stuart T. Weinberg , Mary Anne Whelan , SUBCOMMITTEE ON THE MANAGEMENT OF INFANTILE HEMANGIOMAS Abstract Infantile hemangiomas (IHs) occur in as many as 5% of infants, making them the most common

2019 American Academy of Pediatrics

8. Infantile haemangioma: topical timolol

no NICE guidance on the treatment of infantile haemangioma. References Chakkittakandiyil A, Phillips R, Frieden IJ et al. (2012) Timolol maleate 0.5% or 0.1% gel-forming solution for infantile hemangiomas: a retrospective, multicenter, cohort study. Pediatric Dermatology 29; 28–31 Chan H, McKay C, Adams S, Wargon O (2013) RCT of timolol maleate gel for superficial infantile hemangiomas in 5- to 24-week-olds. Pediatrics 131; e1739 –47 Kumar MG, Coughlin C, Bayliss SJ (2015) Outpatient use of oral (...) Infantile haemangioma: topical timolol Infantile haemangioma: topical timolol Infantile haemangioma: topical timolol Evidence summary Published: 14 August 2015 nice.org.uk/guidance/esuom47 pathways K Ke ey points from the e y points from the evidence vidence The content of this evidence summary was up-to-date in August 2015. See summaries of product characteristics (SPCs), British national formulary (BNF), BNF for children (BNFc) or the MHRA or NICE websites for up-to-date information. Summary

2015 National Institute for Health and Clinical Excellence - Advice

9. Clinical Practice Guideline for the Management of Infantile Hemangiomas Full Text available with Trip Pro

Clinical Practice Guideline for the Management of Infantile Hemangiomas Infantile hemangiomas (IHs) occur in as many as 5% of infants, making them the most common benign tumor of infancy. Most IHs are small, innocuous, self-resolving, and require no treatment. However, because of their size or location, a significant minority of IHs are potentially problematic. These include IHs that may cause permanent scarring and disfigurement (eg, facial IHs), hepatic or airway IHs, and IHs

2019 EvidenceUpdates

10. Hemangioma of the Cavernous Sinus: A Case Series Full Text available with Trip Pro

Hemangioma of the Cavernous Sinus: A Case Series Introduction  Cavernous sinus hemangiomas (CSHs) are rare, vascular, extra-axial tumors that are diagnosed with a combination of imaging and biopsy. We describe the clinical presentations, imaging findings, and management of two male patients with CSHs. Case Report  Case 1 describes a 57-year-old man who presented with vision changes and cranial nerve palsies. Initial imaging and surgical biopsy were nondiagnostic. Follow-up Tc-99m tagged red

2018 Journal of neurological surgery reports

11. Retinal racemose hemangioma with retinal artery macroaneurysm: Optical coherence tomography angiography (OCTA) findings Full Text available with Trip Pro

Retinal racemose hemangioma with retinal artery macroaneurysm: Optical coherence tomography angiography (OCTA) findings To describe a rare case of retinal racemose hemangioma (RRH) with retinal artery macroaneurysm (RAM) and its optical coherence tomography angiography (OCT-A) finding before and after treatment.Congenital arteriovenous (AV) communications or RRH is a rare developmental anomaly associated with various ocular conditions. RRH alone is usually asymptomatic, and vision loss occurs

2018 American journal of ophthalmology case reports

12. Subglottic hemangioma: Understanding the association with facial segmental hemangioma in a beard distribution. (Abstract)

Subglottic hemangioma: Understanding the association with facial segmental hemangioma in a beard distribution. A subglottic hemangioma (SGH) is a benign tumor of infancy that can cause severe obstruction of the airway. Infantile hemangiomas, in general, are the most common head and neck tumor in children, affecting 4-5% of the pediatric population. This retrospective cohort study characterizes subglottic infantile hemangiomas at a single vascular anomaly center over a 5-year period (2013-2017 (...) ) during the era of propranolol treatment.Queried the Vascular Anomaly Database at Children's Hospital of Pittsburgh for all infantile hemangioma(s) and then identified case of subglottic hemangiomas. Characterized key features of presentation, natural history and management for subglottic hemangiomas. A secondary differentiation focused on differences between subglottic hemangiomas associated with Beard Distribution (BD) vs not (NBD).Analysis of 761 cases of infantile hemangiomas demonstrated only 13

2018 International Journal of Pediatric Otorhinolaryngology

13. Atypical hepatic hemangioma: imaging features of hyalinized hemangioma Full Text available with Trip Pro

Atypical hepatic hemangioma: imaging features of hyalinized hemangioma 29898024 2018 07 30 2018 11 14 2317-6385 16 2 2018 Jun 11 Einstein (Sao Paulo, Brazil) Einstein (Sao Paulo) Atypical hepatic hemangioma: imaging features of hyalinized hemangioma. eAI4256 S1679-45082018000200700 10.1590/S1679-45082018AI4256 Nunes Letícia Maria Araujo Oliveira LMAO Hospital Israelita Albert Einstein, São Paulo, SP, Brazil. Mello-Amoedo Caroline Duarte de CD Hospital Israelita Albert Einstein, São Paulo, SP (...) , Brazil. Yamauchi Fernando Ide FI Hospital Israelita Albert Einstein, São Paulo, SP, Brazil. Baroni Ronaldo Hueb RH Hospital Israelita Albert Einstein, São Paulo, SP, Brazil. eng por Case Reports Journal Article 2018 06 11 Brazil Einstein (Sao Paulo) 101281800 1679-4508 IM Hemangioma diagnostic imaging Humans Incidental Findings Liver Neoplasms diagnostic imaging Magnetic Resonance Imaging Male Middle Aged 2017 08 30 2018 01 06 2018 6 14 6 0 2018 6 14 6 0 2018 7 31 6 0 epublish 29898024 S1679

2018 Einstein

14. Propranolol (Hemangiol): the drug of first choice for severe infantile haemangiomas

Propranolol (Hemangiol): the drug of first choice for severe infantile haemangiomas Prescrire IN ENGLISH - Spotlight ''Propranolol (Hemangiol°): the drug of first choice for severe infantile haemangiomas '', 1 July 2015 {1} {1} {1} | | > > > Propranolol (Hemangiol°): the drug of first choice for severe infantile haemangiomas Spotlight Every month, the subjects in Prescrire’s Spotlight. 100 most recent :  |   |   |   |   |   |   |    (...) |   |  Spotlight Propranolol (Hemangiol°): the drug of first choice for severe infantile haemangiomas FEATURED REVIEW Haemangiomas are benign vascular tumours that generally arise in the skin during the first days of life. When an infant requires medical treatment for haemangioma, oral propranolol is the drug of first choice. Full review (3 pages) available for download by subscribers. Abstract Haemangiomas are benign vascular tumours that generally arise in the skin during the first days

2015 Prescrire

15. Cardiac Cavernous Hemangioma Coexisting With Pulmonary Cavernous Hemangiomas and Giant Hepatic Hemangioma. Full Text available with Trip Pro

Cardiac Cavernous Hemangioma Coexisting With Pulmonary Cavernous Hemangiomas and Giant Hepatic Hemangioma. We describe a case of cardiac cavernous hemangioma with coexisting pulmonary cavernous hemangiomas and hepatic hemangioma. A 35-year-old woman who had previously received a living donor liver transplant to cure giant hepatic hemangioma was seen because of chest pain. A cardiac neoplasm and multiple pulmonary nodules were detected. The tumor was surgically removed, and biopsy specimens were (...) taken from the lung nodules. Histopathologic examination confirmed that both lesions were cavernous hemangiomas. The patient was discharged without adverse events postoperatively. Cardiac hemangioma is an extremely rare entity; the present case is unique for its multiorgan involvement. Suspicion of this entity should be aroused if the imaging manifestation suggests a vascular nature.Copyright © 2017 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

2017 Annals of Thoracic Surgery

16. Diagnosis and management of infantile hemangioma

Diagnosis and management of infantile hemangioma Diagnosis and management of infantile hemangioma Diagnosis and management of infantile hemangioma Chinnadurai S, Snyder K, Sathe N, Fonnesbeck C, Morad A, Likis FE, Surawicz T, Ness G, Ficzere C, McPheeters ML Record Status This is a bibliographic record of a published health technology assessment from a member of INAHTA. No evaluation of the quality of this assessment has been made for the HTA database. Citation Chinnadurai S, Snyder K, Sathe N (...) , Fonnesbeck C, Morad A, Likis FE, Surawicz T, Ness G, Ficzere C, McPheeters ML. Diagnosis and management of infantile hemangioma. Rockville: Agency for Healthcare Research and Quality (AHRQ). Comparative Effectiveness Review No. 168. 2016 Authors' objectives To systematically review evidence addressing the diagnosis and management of infantile hemangiomas (IH). Authors' conclusions Our review for contextual questions described a range of indications for referral and suggested support for a higher index

2016 Health Technology Assessment (HTA) Database.

17. Bilateral Renal Anastomosing Hemangiomas: A Tale of Two Kidneys Full Text available with Trip Pro

Bilateral Renal Anastomosing Hemangiomas: A Tale of Two Kidneys Background: Renal anastomosing hemangioma (RAH) is an extremely rare benign vascular tumor first described in 2009. Making this diagnosis is fraught with challenges. Radiologically they share features consistent with renal cell carcinomas (RCCs). Their vascular nature poses risks if considering preoperative biopsy and histologically they share characteristics akin to angiosarcomas. The few reports published in the literature (...) was hemodynamically unstable and, therefore, required an emergency open left-sided nephrectomy, rendering her anephric and dialysis dependent. Postoperative histologic examination proved that the left kidney also contained an RAH. Conclusion: The anastomosing hemangioma is an important subtype to differentiate from angiosarcoma before and after a nephrectomy. Urologists should carefully consider invasive tests in patients with previously diagnosed vascular lesions as there may be an increased risk of bleeding

2017 Journal of endourology case reports

18. Clinical outcomes and predictors of response to photodynamic therapy in symptomatic circumscribed choroidal hemangioma: A retrospective case series. Full Text available with Trip Pro

Clinical outcomes and predictors of response to photodynamic therapy in symptomatic circumscribed choroidal hemangioma: A retrospective case series. To investigate the treatment outcomes and predictors of response to photodynamic therapy (PDT) in patients with symptomatic circumscribed hemangioma (CCH).This retrospective case series examined 20 patients with symptomatic CCH (10 submacular CCHs and10 juxtapapillary CCHs) who underwent standard PDT (wavelength: 662 nm; light dose: 50J/cm2

2018 PLoS ONE

19. Effectiveness of Sorafenib in Hepatic Hemangioma Full Text available with Trip Pro

Effectiveness of Sorafenib in Hepatic Hemangioma 30241175 2019 03 04 2378-9506 4 2018 Sep Journal of global oncology J Glob Oncol Effectiveness of Sorafenib in Hepatic Hemangioma. 1-4 10.1200/JGO.2016.008573 Tiwari Prateek P All authors: Cancer Institute (WIA), Adyar, Chennai, India. Mahajan Vandana V All authors: Cancer Institute (WIA), Adyar, Chennai, India. Muhrerkar Kanchan K All authors: Cancer Institute (WIA), Adyar, Chennai, India. Sunil Bhanu Jayanand BJ All authors: Cancer Institute

2017 Journal of global oncology

20. Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection Full Text available with Trip Pro

Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection Background Lobular capillary hemangioma is a rare benign tumor, most frequently located in the head or neck region, the nasal cavity being uncommonly affected. Its etiopathogenesis is not fully established, although traumatic and hormonal factors have been implied. Case Description A 50-year-old female patient underwent an uneventful endoscopic (...) transsphenoidal removal of a pituitary cystic macroadenoma at our institution. Nasal packing was used in postoperative hemostasis. Histopathology was compatible with a gonadotrophin-producing adenoma. One month after the surgery, the patient presented with frequent episodes of epistaxis and a progressively growing nasal mass, which was removed endoscopically. Its pathological examination confirmed a lobular capillary hemangioma. Conclusions The authors present a clinical case combining two possible

2017 Journal of neurological surgery reports

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