Academic literature on the topic 'Cystic hygroma adult'

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Journal articles on the topic "Cystic hygroma adult"

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Singh, Lt Col I. D., and Maj Abhipsa Hota. "Recurrent cystic hygroma in an adult presenting as a neck mass - A case study." Journal of Medical Research 1, no. 2 (2015): 46–48. http://dx.doi.org/10.31254/jmr.2015.1204.

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Cystic Hygroma although common in children, can also present in adults. It should be managed with great precision because of its proximity to vital anatomy. This case report discusses a rare presentation of a 52 years old adult presenting with cystic hygroma. It illustrates how difficult can cystic hygroma get, especially during dissection. In this case, careful delineation of structures was done to excise the mass without injury to surrounding nerves and vessels. Cystic hygromas do not resolve spontaneously and surgical excision is the treatment of choice in such cases.
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Derin, Serhan, Murat Şahan, Yelda Dere, Neşat Çullu, and Leyla Şahan. "Cervical Cystic Hygroma in an Adult." Case Reports in Pathology 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/209427.

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Cystic hygromas/lymphangiomas are extremely rare malformations in adults. They are usually seen in infants and children under 2 years of age. En bloc resection is difficult due to the adhesive characteristics of the tumors. Inadequate surgical intervention often leads to recurrent disease. We report herein the case of a cystic hygroma/lymphangioma that presented as an uncommon mass on the cervical region in an adult, together with its histopathological, radiologic, and operative features.
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Lodhia, Jay, Atiyya Hussein, Patrick Amsi, Joseph Mtokambali, and David Msuya. "An uncommon delayed presentation of a large cystic hygroma in a teenage girl: a case report." International Journal of Surgery Open 62, no. 5 (2024): 627–30. https://doi.org/10.1097/io9.0000000000000188.

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Cystic hygromas are congenital malformations of lymphatic origin, that are mostly diagnosed in the perinatal period. The term “hygroma” comes from Greek meaning tumor filled with water. They are commonly found in children under 2 years and incidence decreases with age. Due to their diverse presentation, its optimum treatment often poses a potential challenge. There are only a few cases described in the literature of late teen and adult cystic hygromas and their optimum management remains a challenge. In this report, we present a case of large cervical cystic hygroma in a teenage girl with a po
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Karkos, P. D., M. G. Spencer, M. Lee, and B. N. Hamid. "Cervical cystic hygroma/lymphangioma: an acquired idiopathic late presentation." Journal of Laryngology & Otology 119, no. 7 (2005): 561–63. http://dx.doi.org/10.1258/0022215054352144.

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Lymphangiomas or cystic hygromas are relatively uncommon congenital malformations of the lymphatic system which usually present in the first years of childhood. Presentation in adult life is rare. We present a case of cervical adult cystic hygroma and discuss radiological and histopathological features as well as the management of these neck masses.
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Gajbhiye, Raj N., Ganesh K. Kharkate, and Vidhey S. Tirpude. "Transoral endoscopic excision of cystic hygroma vestibular approach in adult (novel approach): a case report." International Surgery Journal 7, no. 9 (2020): 3136. http://dx.doi.org/10.18203/2349-2902.isj20203810.

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Lymphangioma, soft tissue tumor was originally reported by R. Backer in 1828 and “cystic hygroma” name was first given by Wernker in 1834. It can occur in the head, neck, axilla, cervico-facial regions and below tongue. Although it is well recognized in children, it may present in adulthood. Cystic hygroma neck is traditionally removed via an overlying incision near or over the swelling. The resultant scar can be displeasing to an adult. Various endoscopic approach present in literature for excision are via neck, anterior chest, combined or robotic assisted. We here, are reporting transoral en
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Piłkowski, Michał, Józef Komorski, Jan Nienartowicz, and Kamil Nelke. "Cervical Cystic Hygroma in an Older Adult: A case study." Polski Przegląd Otorynolaryngologiczny 9, no. 4 (2020): 1–5. http://dx.doi.org/10.5604/01.3001.0014.5925.

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Cystic hygromas are very uncommon malformations in adults. In most of the cases, they present as a painless, fluctuant swelling, usually located in the neck region. They tend to grow extensively if not removed. Cystic hygromas can range from 1 mm to several centimeters in size and are filled with clear- to straw-colored fluid. Surgical treatment remains the gold-standard treatment for these tumors. In some cases they can be misdiagnosed with branchial cysts, swollen lymph nodes or other pathologies. When this malformation is present in the prevertebral fascia its surgical treatment is challeng
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Siguan, Stephen Sixto, and Mary Nicole Velez. "Adult-Onset Cystic Hygroma in the Axilla in a 44-year old Female: A Case Report." Philippine Journal of Surgical Specialties 74, no. 2 (2019): 44–49. http://dx.doi.org/10.61662/pcs_dzft1350.

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This is a case of a 44- year old female presenting with an 18cm x 17cm soft, movable, non-tender mass at the right axilla extending to the lateral aspect of the right breast. Computerized tomographic scan of the chest revealed a lobulated, multi-septated hypodense mass. The patient underwent excision of the right axillary mass and final histopathology revealed cystic lymphangioma. Adult-onset cystic hygroma of the axilla is a rare case, with less than 10 studies documented in PubMed. Total surgical excision remains to be its primary treatment. Key words: Adult-onset cystic hygroma, cystic hygr
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Kadam, Sachin S., and Tejaswini Kadam. "Cystic hygroma in a young adult: A case report and recent management." Tumor Discovery 1, no. 2 (2022): 151. http://dx.doi.org/10.36922/td.v1i2.151.

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We are reporting a case of a 27-year-old young female who presented with right side neck swelling without any associated obstructive symptoms and any other grave signs and symptoms. She noticed a gradual increase in the size of the swelling within a period of 2 years. After investigation and surgical excision, the swelling was diagnosed as cystic hygroma. The root cause of the development of cervical lymphangioma is the congenital malformation of the developing lymphatic system. Cystic hygroma is benign in nature and the cause in adults is still unclear. The most common site of origin is in he
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Chabaria, Rachana. "Huge adult cystic hygroma: anaesthesia challenge." International Journal of Otorhinolaryngology and Head and Neck Surgery 1, no. 1 (2015): 52. http://dx.doi.org/10.18203/issn.2454-5929.ijohns20150590.

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Cystic hygroma is a rare lymphatic tumor, uncommonly seen in adults. We report a case of woman aged 55 years, who presented with a huge cystic swelling causing difficulty in neck movements. Huge neck swelling distorting the anatomy poses a challenge for securing the airway. The airway was secured with orotracheal intubation with help of a bougie after general anaesthesia, shifting the swelling off the midline by an experienced anaesthesiologist. Appropriate preoperative airway assessment, meticulous planning anticipating difficulty and simple manoeuvres, can ease intubation.
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Prasad, Amarendra, Srikanth Raju, Srinivasa Karthik, Gaje Venu, and Mithun. "Adult Cystic Hygroma– A Rare Entity." Indian Journal of Mednodent and Allied Sciences 3, no. 1 (2015): 55. http://dx.doi.org/10.5958/2347-6206.2015.00013.8.

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Conference papers on the topic "Cystic hygroma adult"

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Gomes, Vinicius de Aquino Calasso Correa, Gil Facina, Simone Elias, and Joaquim Teodoro de Araujo Neto. "RELAPSING AXILLARY LYMPHANGIOMA IN AN ELDERLY PATIENT: CASE REPORT AND LITERATURE REVIEW." In Scientifc papers of XXIII Brazilian Breast Congress - 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s1084.

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Introduction: Lymphangioma or cystic hygroma is a rare and benign lesion usually found in children or newborns, hardly described after two years of age. It is characterized by congenital obstruction of the lymphatic vessels, which causes dilation and accumulation of lymph inside it. In adults, it can be secondary to trauma and can occur in the neck, head and, more rarely, in the breast and armpit3 . In this study we present an atypical case of recurrent axillary lymphangioma in an elderly patient. Case report: Female patient, 71 years old, with no history of neoplasms, was referred to the brea
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