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MRI Features And Treatment Of Pharyngeal Haemangioma

机译:咽部血管瘤的MRI特征及治疗

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Pharyngeal haemangioma is a comparatively a rare tumor of the head and neck region . The treatment modalities include surgical removal , sclerotherapy and laser therapy . We report a case of large pharyngeal haemangioma extending from the hypopharynx to the oropharynx. A 60- year old male presented with progressive dysphagia of 1- year duration . A large pharyngeal haemangioma was diagnosed on laryngoscopy and magnetic resonance imaging . Sclerotherapy using 5% mono ethanolamine oleate decreased the tumor volume immediately , without showing any tendency to re grow during last 18 months of follow up . Introduction Haemangiomas are generally considered to be developmental malformations or hamartomas rather than true neoplasm . In the year 1904 , Albrechet defined hamartomas as a tumor like malformation composed of tissue indigenous to the part, but lacking the growth potential of the neoplasm . Haemangiomatous lesions may arise in the skin or anywhere in the mucosa of the upper aero-digestive tract ( 1 ).The most likely vasoformative tumor to be submitted for biopsy from the oral or pharyngeal region is the haemangioma ( 2 ). Most true Haemangiomas require no intervention , but 10 – 20 % requires treatment because of their size , location , behavior , degree of functional compromise or complications . The treatment options include conservative management by monitoring , steroids , cryotherapy , laser therapy , sclerotherapy , and surgical excision ( 3 , 4 ). Case Report A 60- year old male presented with the complaint of progressive dysphagia for last one year , which was more for solid food than for liquids . There was no history of haematemesis , dyspnoea , haemoptysis , or hoarseness of voice . Indirect laryngoscopy revealed a purple coloured pharyngeal mass , “4 × 2 cm” in size , arising from right lateral wall . Laboratory investigations were normal . Direct laryngoscopic examination confirmed a broad based purplish lobulated mass , about “5 × 2 cm” in size with intact overlying mucosa , arising from the right lateral wall of the hypopharynx . It was extending superiorly into oropharynx Prominent vessels and scattered areas of haemorrhage were seen over its surface . A wedge biopsy was taken from the mass , which confirmed the diagnosis of haemangioma . There were no pheleboliths within the tumor . M R I revealed a well defined lobulated hyper intense mass lesion about “5 x 2 cm” arising from right lateral wall of hypopharynx with a broad base , extending cranially into oropharynx “( fig 1 )”. In T1-WI the lesion was iso-intense to muscles ( fig 2 )”. Post-Gadolium images “( fig 3 & 4 )” show heterogeneous and significant enhancement . The patient was subjected to sclerotherapy using 5% mono ethanolamine oleate under general anaesthesia . The tumor decreased in volume immediately after sclerotherapy . The patient is on regular follow-up since last 18 - months , and has not shown any tendency to increase its volume .
机译:咽部血管瘤是一种相对罕见的头颈部肿瘤。治疗方式包括手术切除,硬化疗法和激光疗法。我们报告了一例从咽下到口咽的大咽部血管瘤。一名60岁的男性表现为持续1年的进行性吞咽困难。通过喉镜和磁共振成像诊断出较大的咽部血管瘤。使用5%单乙醇胺油酸酯的硬化治疗立即减少了肿瘤的体积,在随访的最后18个月中没有出现再生长的趋势。引言血管瘤通常被认为是发育畸形或错构瘤,而不是真正的肿瘤。在1904年,Albrechet将错构瘤定义为一种由畸形形成的肿瘤,由部分固有组织组成,但缺乏赘生物的生长潜力。血管瘤性病变可能出现在皮肤或上消化道粘膜的任何地方(1)。最可能从口腔或咽部区域进行活检的血管形成性肿瘤是血管瘤(2)。大多数真正的血管瘤不需要干预,但由于其大小,位置,行为,功能损害程度或并发症,因此需要治疗的患者占10%至20%。治疗选择包括通过监测,类固醇,冷冻疗法,激光疗法,硬化疗法和手术切除的保守治疗(3,4)。病例报告一名60岁男性最近一年患有进行性吞咽困难,其中固体食物多于液体。没有呕血,呼吸困难,咯血或声音嘶哑的历史。间接喉镜检查发现右侧咽侧壁出现紫色咽肿块,大小为“ 4×2 cm”。实验室检查是正常的。直接的喉镜检查证实了一个宽阔的紫色小叶状肿块,大小约为“ 5×2 cm”,完整的粘膜覆盖于下咽右侧壁。它向上延伸到口咽。突出的血管可见散在的出血区域。从肿块进行楔形活检,证实了血管瘤的诊断。肿瘤内没有石柱石。 M R I揭示了一个清晰的小叶高肿块病变,大约在“ 5 x 2 cm”处,起源于下咽右侧壁,底部宽阔,颅骨延伸到口咽处(图1)。在T1-WI中,病变对肌肉等强度(图2)”。 G后图像“(图3和4)”显示出异质且显着的增强。该患者在全身麻醉下使用5%单乙醇胺油酸酯进行硬化治疗。硬化治疗后肿瘤体积缩小。自最近18个月以来,该患者一直接受定期随访,并且未显示出增加其容量的任何趋势。

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