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Gotowe bibliografie tematyczne / Facial teratoma

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Gotowa bibliografia na temat „Facial teratoma”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Facial teratoma"

1

Gao, Chuan-Fen, Pei Zhou, and Chen Zhang. "Prenatal ultrasound diagnosis of fetal maxillofacial teratoma: Two case reports." World Journal of Clinical Oncology 15, no. 9 (2024): 1245–50. http://dx.doi.org/10.5306/wjco.v15.i9.1245.

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BACKGROUND Facial teratoma is a rare benign tumor that accounts for about 1.6% of all teratomas and can be diagnosed by prenatal ultrasound (US). The purpose of this report was to describe our experience with the diagnosis of fetal facial teratoma by prenatal US at second trimester to provide a reference for clinical diagnosis of fetal maxillofacial teratoma. CASE SUMMARY We present two cases of patients with abnormal fetal facial findings on US at second trimester of pregnancy in our department. Case 1 was a 31-year-old G3 P1 + 1 female, with US revealing a heterogeneous echogenicity of 32 mm

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Bouguermouh, Dania, Said Boutemeur, and Fatma Hamel. "Oropharyngeal teratoma in a newborn: A case report." Journal of Neonatal Surgery 12 (December 5, 2023): 31. http://dx.doi.org/10.47338/jns.v12.1187.

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Background: Facial teratomas are rare congenital tumors in the craniocervical region. They constitute only 2-5% of all childhood teratomas. Case Presentation: This report presents a case of an oral teratoma in an infant, attached to the palate and extending sublingually on the right side, along with a cleft palate. The patient underwent successful surgical excision on the 17th day of life performed by a team of pediatric and maxillofacial surgeons. Conclusion: The case emphasizes the importance of interdisciplinary coordination for the management of facial teratomas, involving maxillofacial an

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Rai, Manjunath, Padmaraj Hegde, and Umesh M. Devaraju. "Congenital Facial Teratoma." Journal of Maxillofacial and Oral Surgery 11, no. 2 (2011): 243–46. http://dx.doi.org/10.1007/s12663-011-0186-0.

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Solis-Pazmino, Paola, Vanessa Solano, Camila Pazmino-Chavez, and Cristhian Garcia. "Large congenital facial teratoma." BMJ Case Reports 16, no. 4 (2023): e253318. http://dx.doi.org/10.1136/bcr-2022-253318.

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This case report discusses a presentation of a giant facial teratoma, a rare congenital neoplasm. Head and neck locations of the tumour uncommonly distort the face and may be associated with functional problems. We present a case of teratoma arising from the right parotid extending to the extracranial regions, successfully managed by surgical resection. Reviewing this case with the supporting body of literature anticipates further investigation to address patients’ needs more thoroughly.

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Chaudhary, Neena, Krishna Pal Singh Malik, Alok Gupta, Anil Kumar Rai, Pankaj Gupta, and Geetika Khanna. "Synchronous cystic teratomas of the craniofacial region." Journal of Laryngology & Otology 117, no. 10 (2003): 824–26. http://dx.doi.org/10.1258/002221503770716296.

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A case of synchronous cystic teratomas presented with the complaints of a slow-growing facial mass and forward protrusion of the right eye since birth. The patient was examined thoroughly and subjected to magnetic resonance imaging (MRI) scan. The MRI scan revealed the presence of two separate cysts in the right orbit and right temporal fossa. The patient was operated by a combined effort of ophthalmologists and otorhinolaryngologists. The cysts were excised and subjected to pathological examination. The histopathological survey revealed both the cysts to be mature cystic teratomas similar to

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Mpayo, Lucy Lawrence, Aslam Nkya, Shabani Mawalla, and Karim Premji Manji. "Post-auricular teratoma in an HIV-exposed newborn." BMJ Case Reports 16, no. 2 (2023): e252977. http://dx.doi.org/10.1136/bcr-2022-252977.

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Teratomas in the neonatal age group are mostly benign at first, and the common site is the sacrococcygeal region. They are rarely associated with HIV infection. We report a case of an HIV-exposed newborn with a congenital teratoma at the post-auricular site who developed an infection. Early intervention by total surgical resection will prevent complications such as infections and malignant transformation. A term baby was delivered spontaneously by an HIV-positive mother who was on her regular medications. Prenatal ultrasound carried out in the third trimester showed a cyst swelling on the righ

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7

Nadia, Ben Jamaa, Achour Radhouane, Ayari Feirouz, et al. "Facial Teratoma in the Newborn: Diagnosis and Prognosis." Annual Research & Review in Biology 13, no. 2 (2017): 1–4. https://doi.org/10.9734/ARRB/2017/33890.

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Facial teratoma is an extremely rare germinal tumor in newborn babies. It is often diagnosed antenatally by means of ultrasound and even MRI. The prognosis of this tumor depends mainly on the size and the location of the lesion (eye, respiratory and digestive tracts). Multidisciplinary examination is needed to ensure the newborn’s survival. Pre-operative conditioning is needed to avoid complications and carcinogenic risks. The aim of this article is to Specify the anatomical features of facial teratoma and consider the interests of foetopathology review. We report a male baby, prematurely born

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8

Siddiqui, H. F., and S. Anjum. "A fetus with a mass in the oral cavity: a rare case of large oral immature teratoma." American Journal of Clinical Pathology 162, Supplement_1 (2024): S138. http://dx.doi.org/10.1093/ajcp/aqae129.306.

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Abstract Introduction/Objective Oral teratoma is a rare congenital neoplastic lesion composed of variable amounts of all three germ cell layers, comprising 2-9% of all teratomas. Teratomas are classified into subtypes depending upon the presence of immature components. Sacrococcygeal and head and neck regions are the most common sites, with slight female predominance. Mortality increases if diagnosed in the fetal or neonatal period. Methods/Case Report We report a case of male fetus diagnosed radiologically as ultrasound at 20 weeks of gestation revealed abnormal facial characteristics. A huge

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9

Van Goethem, Bart, Tim Bosmans, and Koen Chiers. "Surgical Resection of a Mature Teratoma on the Head of a Young Cat." Journal of the American Animal Hospital Association 46, no. 2 (2010): 121–26. http://dx.doi.org/10.5326/0460121.

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A 4-month-old kitten was presented with a large mass over the temporal area involving the base of the left ear. Cytological evaluation of a fine-needle aspirate was not diagnostic. Computed tomography was used to determine tumor extent. Surgical resection was performed, which included parts of the orbital rim, masticatory muscles, the complete ear canal, and the pinna. Reconstruction of the ocular muscles was performed, and the skin defect was reconstructed using a single pedicle advancement flap. Despite unilateral facial paralysis, postoperative clinical function was excellent and aesthetics

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Gharaibeh, Mahmoud M., Ahmed Al Wadiya, Ahmad Gharaibeh, and Hdua Hammad. "Rare Benign cystic teratoma in the parotid gland." European Journal of Clinical and Experimental Medicine 18, no. 1 (2020): 42–44. http://dx.doi.org/10.15584/ejcem.2020.1.9.

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Introduction. A teratoma is a tumor developed of several different types of tissue, like hair, muscle, teeth or bone. Aim. Mature benign cystic teratomas are very rare in the salivary glands and just few cases were reported. Description of the case. A 13 years old female was presented to our dental clinic of Princes Basma Hospital in Irbid in north of Jordan, with a painless, insidious progressive swelling in left parotid region without any significant family and personal history. Parents were cancer phobic and nervous from the condition of their daughter, they were very confused. There was no

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Części książek na temat "Facial teratoma"

1

Achour, Radhouane, and Nadia Ben Jamaa. "Facial Teratoma in the Newborn: A Preventable Disease?" In Medical Research and Its Applications Vol. 3. B P International, 2024. http://dx.doi.org/10.9734/bpi/mria/v3/144.

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Shah, Shailee S., and Marie F. Grill. "Rapidly Progressive Memory Loss, Mood Change, Mutism, and Abnormal Movements." In Mayo Clinic Cases in Neuroimmunology, edited by Andrew McKeon, B. Mark Keegan, and W. Oliver Tobin. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780197583425.003.0025.

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A 24-year-old woman sought care for 2 weeks of disorientation and short-term memory difficulties, as well as diffuse tremor of all extremities. She returned with further decline in memory and new severe headaches. She had intermittent agitation and emotional outbursts of crying or laughing, insomnia, spells consisting of disorganized speech and episodes of intermittent right gaze deviation with facial twitching and lip smacking. She was nearly mute. Her appetite had decreased and she had not had a bowel movement in several days. She was noted to have significant tachycardia and was intermitten

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