Log in

Relevant bibliographies by topics / Facial teratoma / Journal articles

To see the other types of publications on this topic, follow the link: Facial teratoma.

Journal articles on the topic 'Facial teratoma'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Facial teratoma.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

11

Kim, Y., H. Won, and M. Lee. "EP11.02: Prenatal diagnosis of huge facial teratoma." Ultrasound in Obstetrics & Gynecology 52 (October 2018): 243. http://dx.doi.org/10.1002/uog.19962.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

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

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Tobias, Samuel, Javier Valarezo, Karen Meir, and Felix Umansky. "Giant Cavernous Sinus Teratoma: A Clinical Example of a Rare Entity: Case Report." Neurosurgery 48, no. 6 (2001): 1367–71. http://dx.doi.org/10.1097/00006123-200106000-00041.

Full text

Abstract:

Abstract OBJECTIVE AND IMPORTANCE Teratomas represent 0.5% of all intracranial tumors. These benign tumors have tissue representative of the three germinal layers: ectoderm, mesoderm, and endoderm. Most teratomas are midline tumors located predominantly in the sellar and pineal regions. Cavernous sinus location is very rare; only two purely intracavernous teratomas have been reported. CLINICAL PRESENTATION A 14-year-old boy presented with a history of progressive right eye proptosis and visual acuity impairment, headaches, and a neuralgia-like facial pain in the right V1 distribution. A head c

APA, Harvard, Vancouver, ISO, and other styles

14

Cunchillos, Manuel Navarro, María Dolores Calvo Bonachera, Myriam Navarro Cunchillos, Elisa Cassinello, Julio Ramos Lizana, and José Oña Esteban. "Middle ear teratoma in a newborn." Journal of Laryngology & Otology 110, no. 9 (1996): 875–77. http://dx.doi.org/10.1017/s0022215100135212.

Full text

Abstract:

AbstractTeratomas are tumours that rarely exist in children. Their location in head and neck is, however, an unusual finding.A strange case of middle ear congenital teratoma reaching the cervical area is presented here. In the last 20 years it is only the second case to be published in the English literature. The tumour was revealed by the presence of a peripheral congenital facial palsy.

APA, Harvard, Vancouver, ISO, and other styles

15

Kajananan, S., J. A. K. Udeshika, Anuradha Jayakody, M. D. S. Lokuhetty, and Bimsara Senanayake. "Rapid deterioration of a case of anti–N-methyl-D-aspartate receptor encephalitis with an ovarian teratoma, mimicking viral encephalitis." Jaffna Medical Journal 35, no. 1 (2023): 27–30. http://dx.doi.org/10.4038/jmj.v35i1.181.

Full text

Abstract:

Anti–N-methyl-D-aspartate receptor (NMDAR) encephalitis has recently emerged as an autoimmune encephalitis syndrome. Younger females are more likely to develop this condition which usually presents as a multistage illness with predominant neuropsychiatric manifestations. It is associated with the neuroglial surface antibodies developing against NMDAR. The association of ovarian teratoma has been well recognised in this condition and tumour resection will intensify the recovery of the illness along with immunotherapy. We present a case of 19-year-old female who presented with acute onset of fev

APA, Harvard, Vancouver, ISO, and other styles

16

Ikeguchi, Ryotaro, Yuko Shimizu, Ayato Shimomura, et al. "Paraneoplastic AQP4-IgG–Seropositive Neuromyelitis Optica Spectrum Disorder Associated With Teratoma." Neurology - Neuroimmunology Neuroinflammation 8, no. 5 (2021): e1045. http://dx.doi.org/10.1212/nxi.0000000000001045.

Full text

Abstract:

ObjectivesTo assess a case of paraneoplastic aquaporin-4 (AQP4)-immunoglobulin G (IgG)–seropositive neuromyelitis optica spectrum disorder (NMOSD) associated with teratoma and determine whether it is a paraneoplastic neurologic disorder.MethodsA single case study and literature review of 5 cases.ResultsA 27-year-old woman presented with diplopia, facial nerve palsy, paraplegia, sensory dysfunction of lower limbs, dysuria, nausea, and vomiting. Spinal cord MRI detected an extensive longitudinal lesion in the spinal cord, and brain MRI detected abnormal lesions in the right cerebral peduncle and

APA, Harvard, Vancouver, ISO, and other styles

17

Kekre, Geeta, Abhaya Gupta, Paras Kothari, et al. "Congenital facial teratoma in a neonate: Surgical management and outcome." Annals of Maxillofacial Surgery 6, no. 1 (2016): 141. http://dx.doi.org/10.4103/2231-0746.186140.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Yhoshu, Enono, Gyanendra Chaudhary, Intezar Ahmed, and ManishKumar Gupta. "Congenital lateral facial teratoma: A case report and review of literature." African Journal of Paediatric Surgery 18, no. 2 (2021): 99. http://dx.doi.org/10.4103/ajps.ajps_77_20.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Rattan, Kamal Nain, Simmi K. Ratan, Dhiraj Parihar, Vivek Kaushal, and Samar Pal Yadav. "Giant Neonatal Cervical Teratoma Associated with Facial Clefts-A Rare Association." Journal of Otolaryngology 36, no. 03 (2007): E19. http://dx.doi.org/10.2310/7070.2006.0081.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

M.S, Yadukrishnan, Rita Zarina A., Padmakumari B., and Danu Dayakar P.S. "LABIO-ALVEOLAR MOULDING FOR ESTHETIC AND FUNCTIONAL REHABILITATION OF OROPHARYNGEAL TERATOMA INDUCED SKELTAL AND SOFT TISSUE DEFORMITY IN NEWBORN - A CASE REPORT." International Journal of Advanced Research 11, no. 09 (2023): 95–100. http://dx.doi.org/10.21474/ijar01/17509.

Full text

Abstract:

Teratomaare true neoplasms composed of tissue derived from all the three germinal layers.Teratomas arising in the palate pharynx or tongue and protrude from the mouth can result in life-threatening airway obstruction and feeding difficulties.Surgical excision improves the chance of survival of the newborn but it results in deformation of oral and masticatory apparatus. This article discusses about the role of pediatric dentist in reestablishing the form and function of the facial apparatus following surgical excision of intraoral teratoma.

APA, Harvard, Vancouver, ISO, and other styles

21

Kelemen, Noemi, Ashley Mota, Robert D. Bains, and Mark I. Liddington. "Large Congenital Facial Teratoma Associated With Neurological Migration Disorder (Polymicrogyria) and Absent Corpus Callosum." Journal of Craniofacial Surgery 32, no. 1 (2020): e43-e45. http://dx.doi.org/10.1097/scs.0000000000006879.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Chatzis, I., A. S. Kondylios, I. Varvarigos, G. Farmakides, and S. Sotiriou. "P07.04: A rare case of facial teratoma appearing in the 26th week of pregnancy." Ultrasound in Obstetrics & Gynecology 42, s1 (2013): 138. http://dx.doi.org/10.1002/uog.13001.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Le Saux, A., M. L. Poli Merol, D. Zachar, et al. "Cleft palate associated with cervico-facial teratoma: Report of two cases and review of the literature." International Journal of Pediatric Otorhinolaryngology 76, no. 8 (2012): 1225–27. http://dx.doi.org/10.1016/j.ijporl.2012.05.011.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Yurochko, Fedir, Vasyl Olashyn, and Dzvenyslava Kopanska. "Surgical treatment of a nasal dermoid cyst: open rhinoplasty." Polski Przegląd Otorynolaryngologiczny 8, no. 2 (2019): 49–53. http://dx.doi.org/10.5604/01.3001.0013.1528.

Full text

Abstract:

Midline nasal congenital masses are a rare congenital anomaly. Most often such defects include: vascular tumors, benign and malignant tumors and inflammatory lesions, however the most common are: gliomas, dermoid cysts and hemangiomas. Dermoid cysts (or dermoids) are a benign tumor belongs to choristom group (teratoma). Nasal dermoid cysts (NDCs) are the most common congenital defect of the nasal midline. The diagnosis is usually established at an early age - mainly by the age of 3. Due to late diagnosis and/or delay surgical treatment, facial deformities, recurrent infections (festering of cy

APA, Harvard, Vancouver, ISO, and other styles

25

Hodges, Maggie M., Timothy M. Crombleholme, Ahmed I. Marwan, et al. "Massive facial teratoma managed with the ex utero intrapartum treatment (EXIT) procedure and use of a 3-dimensional printed model for planning of staged debulking." Journal of Pediatric Surgery Case Reports 17 (February 2017): 15–19. http://dx.doi.org/10.1016/j.epsc.2016.11.013.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Siu, Alan, Michaela Lee, Robert Rice, and John S. Myseros. "Association of cerebellopontine angle atypical teratoid/rhabdoid tumors with acute facial nerve palsy in infants." Journal of Neurosurgery: Pediatrics 13, no. 1 (2014): 29–32. http://dx.doi.org/10.3171/2013.10.peds13292.

Full text

Abstract:

Atypical teratoid/rhabdoid tumors (AT/RTs) are highly malignant CNS tumors found almost exclusively in childhood. Although essentially universally fatal when incompletely resected, prompt diagnosis followed by early chemoradiation can improve outcomes. An AT/RT can occur extraaxially at the cerebellopontine angle (CPA) and cause acute cranial nerve deficits as the presenting sign. The authors report a series of 3 children who presented with isolated acute facial nerve palsies and in whom subsequent diagnosis of a CPA AT/RT was made. The authors propose that in young children whose presenting s

APA, Harvard, Vancouver, ISO, and other styles

27

Yu, Fang, Florence Chiang, and Carlos Bazan. "Atypical teratoid/rhabdoid tumor arising from the trigeminal nerve in an adult." Neuroradiology Journal 29, no. 6 (2016): 447–49. http://dx.doi.org/10.1177/1971400916654319.

Full text

Abstract:

A 30-year-old male presented with left facial pain and numbness. Initial MRI demonstrated an enhancing mass involving the left trigeminal nerve. Follow-up imaging showed interval growth with erosion of the sphenoid body. Surgical resection was performed and immunohistochemistry staining was consistent with an atypical teratoid/rhabdoid tumor. Awareness of this entity and its imaging features such as diffusion restriction, intratumoral hemorrhage, and bony destruction, can help guide confirmatory diagnostic testing and appropriate therapy.

APA, Harvard, Vancouver, ISO, and other styles

28

Hadri, Hafssa El, Khaoula Nini, Zakaria Aziz, and Nadia Mansouri Hattab. "Teratoid Cyst of the Floor of the Mouth: Case Report." SAS Journal of Surgery 10, no. 04 (2024): 497–500. http://dx.doi.org/10.36347/sasjs.2024.v10i04.022.

Full text

Abstract:

Dermoid cysts are rare benign tumors of ectodermal origin, they are found in service-facial region with 7% of cases [1]. Floor of the mouth dermoid cysts is even more rare, and are generally localized in the median line of the genioglossus muscle [2]. They are classified as epidermoid cyst, real dermoid cyst and treated depending on the presence or not of the three embryologic contingents. We report the case of a giant congenital teratoid cyst of the floor of the mouth in a 5yo child.

APA, Harvard, Vancouver, ISO, and other styles

29

Gómez Díaz, Oswaldo J., and Mario D. Cruz Sánchez. "Sequence of Surgical Reconstruction in a Child With Cleft Lip and Palate Associated With Congenital Facial Teratomas." Journal of Craniofacial Surgery 28, no. 4 (2017): 1030–34. http://dx.doi.org/10.1097/scs.0000000000003536.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Judd, Dallin, Kaith K. Almefty, Tamara Z. Vern-Gross, et al. "ATRT-08. ATYPICAL TERATOID RHABDOID TUMOR IN AN ADULT PATIENT WITH DOWN SYNDROME." Neuro-Oncology 26, Supplement_4 (2024): 0. http://dx.doi.org/10.1093/neuonc/noae064.008.

Full text

Abstract:

Abstract BACKGROUND Atypical teratoid/rhabdoid tumor (ATRT) is a malignant, highly aggressive embryonal tumor of the central nervous system. Long-term survival remains dismal despite aggressive multimodal therapy, including a maximal safe surgical resection and intensive systemic chemotherapy +/- radiation therapy. While these tumors typically present in infancy or early childhood, there are scattered case reports of adult-onset ATRT. Making prognostic conclusions or therapeutic decisions for this older patient population remains challenging due to the paucity of these reports. CASE REPORT A 2

APA, Harvard, Vancouver, ISO, and other styles

31

Holman, Michelle A., William R. Schmitt, Matthew L. Carlson, Colin L. W. Driscoll, Charles W. Beatty, and Michael J. Link. "Pediatric cerebellopontine angle and internal auditory canal tumors." Journal of Neurosurgery: Pediatrics 12, no. 4 (2013): 317–24. http://dx.doi.org/10.3171/2013.6.peds1383.

Full text

Abstract:

Object The aim in this study was to describe the clinical presentation, differential diagnosis, and risk for neurofibromatosis Type 2 (NF2) in pediatric patients presenting with cerebellopontine angle (CPA) and internal auditory canal (IAC) tumors. Methods The authors conducted a retrospective study at a tertiary care academic referral center. All patients with an age ≤ 18 years who had presented with an extraaxial CPA or IAC tumor between 1987 and 2012 were included in the study cohort. Data regarding symptoms, diagnosis, tumor characteristics, and NF2 status were collected and analyzed. Resu

APA, Harvard, Vancouver, ISO, and other styles

32

Instituto Nacional de Câncer José de Alencar Gomes da Silva. "VIII Congresso Mundial de Cirurgia Oncológica; VIII Congresso Brasileiro de Cirurgia Oncológica; V GASTRINCA; I Simpósio de Enfermagem em Cirurgia Oncológica." Revista Brasileira de Cancerologia 56, no. 1 (2010): 103–34. http://dx.doi.org/10.32635/2176-9745.rbc.2010v56n1.1540.

Full text

Abstract:

Resumos escolhidos para publicação. Nessa edição, os títulos foram: Traquelectomia Radical Abdominal para Tratamento do Câncer do Colo do Útero Invasor: Relato de Caso; Hemipelvectomia: Experiência do Hospital Erasto Gaertner com 32 Casos em Dez Anos; Fístula Anastomótica Pós-Esofagogastrectomia com Anastomose Intratorácica: Experiência do Hospital Erasto Gaertner/Curitiba; A Edição de Livros Técnico-Científicos no INCA; Changing Surgical Strategies after Imatinib Neoadjuvant Therapy: Case Report; The Importance of Clinical Suspicion on the Diagnosis and Treatment of Hereditary Colorectal Canc

APA, Harvard, Vancouver, ISO, and other styles

33

Solis Pazmiño, Andrea Paola, Camila Pazmino-Chavez, Vanessa Solano, and Cristhian Garcia. "THU519 Large Congenital Facial Teratoma: A Case Report." Journal of the Endocrine Society 7, Supplement_1 (2023). http://dx.doi.org/10.1210/jendso/bvad114.2147.

Full text

Abstract:

Abstract Disclosure: A.P. Solis Pazmiño: None. C. Pazmino-Chavez: None. V. Solano: None. C. Garcia: None. Background: Craniocervical teratomas are congenital tumors that arise from the endoderm, mesoderm, and ectoderm germ cell layers. In order to have adequate and prompt management for better outcomes, information about its clinical manifestations and prenatal assessment must be widely disseminated because it can cause death in neonatal patients. The purpose of this case report is to deepen understanding of craniocervical teratoma because there is a dearth of information on the subject. Clini

APA, Harvard, Vancouver, ISO, and other styles

34

Lal, Rohit, and Vinit Kumar Thakur. "Epignathus with Cervical Lymphangioma." Journal of Indian Association of Pediatric Surgeons, August 23, 2024. http://dx.doi.org/10.4103/jiaps.jiaps_41_24.

Full text

Abstract:

Abstract The occurrence of teratoma is 1 in 4,000 live births. Head-and-neck region teratoma (epignathus) is rare. These patients present with facial disfigurement, respiratory problems, and difficulty in feeding. It warrants early excision to avoid any morbidity or mortality due to airway obstruction. We describe the management of a patient with pedunculated epignathus with cervical lymphangioma.

APA, Harvard, Vancouver, ISO, and other styles

35

Morales, Carrie Z., Jessica Blum, Linda M. Saikali, et al. "Prenatal Diagnosis and Staged Reconstruction of a Large Oropharyngeal Teratoma: A Longitudinal Case Report." FACE, January 31, 2025. https://doi.org/10.1177/27325016251315486.

Full text

Abstract:

Introduction: An oropharyngeal teratoma, or epignathus, is a congenital tumor, most commonly found in neonates, that is believed to result from abnormal migration of primordial cells in the mediastinum or hypothalamic regions. Although benign, a feared complication of an epignathus is neonatal airway obstruction, thereby necessitating aggressive airway management and thorough resection. Methods: We report the case of a 19 week and 2 day old fetus prenatally diagnosed with an oropharyngeal teratoma. We describe this patient’s surgical trajectory from birth through the most recent stages of orop

APA, Harvard, Vancouver, ISO, and other styles

36

Shrestha, Ashish Lal, Dakshata Shakya, Sagar Khadka, and Pranita Gurung. "A Finger on the Chin: Rare Report of a Faciomandibular Teratoma in a Nepalese Infant." Case Reports in Pediatrics 2025, no. 1 (2025). https://doi.org/10.1155/crpe/9921032.

Full text

Abstract:

Background: Teratoma is a tumor usually consisting of tissues derived from multiple germ layers. A congenital teratoma occurring in the region of the head and neck is rare with barely 10 reports in the global literature since 1996. Of further rarity is its mandibular location. This probably represents the first report of its kind in the world in addition to being the first one to be reported from Nepal.Case Presentation: We report a case of an 11‐month‐old infant with a congenital appendage over the side of the chin that was treated with surgical excision and histologically confirmed as mature

APA, Harvard, Vancouver, ISO, and other styles

37

Smet, Maria‐Elisabeth, Toni Shurmer, Gregory Kesby, and Andrew McLennan. "Prenatal Diagnosis of a Facial Teratoma. A Proposed Approach to Diagnose Prenatal Facial Anomalies." Journal of Ultrasound in Medicine, November 11, 2020. http://dx.doi.org/10.1002/jum.15564.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Hallenberger, Tim J., Emma von Seth, Michel Roethlisberger, Raphael Guzman, and Jehuda Soleman. "Pituitary germinoma after resection of a mature third ventricular teratoma: illustrative case." Journal of Neurosurgery: Case Lessons 8, no. 2 (2024). http://dx.doi.org/10.3171/case2443.

Full text

Abstract:

BACKGROUND Metachronous intracranial germ cell tumors (iGCTs)—unrelated, histologically different iGCTs occurring at different time points—occurring within the same patient remain a rarity. Herein, the authors report such a case and discuss the literature and potential pathophysiological mechanisms leading to this phenomenon. OBSERVATIONS A 9-year-old boy presented with new-onset impaired balance, headaches, nausea, visual disturbances, and left facial paresis. Magnetic resonance imaging (MRI) scans revealed a suspected pineal region teratoma originating from the pineal gland with consecutive

APA, Harvard, Vancouver, ISO, and other styles

39

Tsoutsanis, Panagiotis A., and George C. Charonis. "Congenital orbital teratoma: a case report with preservation of the globe and 18 years of follow-up." BMC Ophthalmology 21, no. 1 (2021). http://dx.doi.org/10.1186/s12886-021-02229-2.

Full text

Abstract:

Abstract Background Congenital orbital teratomas are extremely rare, usually benign neoplasms, comprised of cells originating from all three germ cell layers. Clinically the tumor appears solid, most of the times is intraconal and presents as a rapidly growing mass leading to a massive unilateral axial proptosis, chemosis, exposure keratopathy, markedly distended eyelids and often, loss of vision. To prevent these complications, tumor excision usually involves enucleation or even orbital exenteration. Case presentation We report a case of a 1-day old infant who presented with dramatic proptosi

APA, Harvard, Vancouver, ISO, and other styles

40

Start, Alex O., Gillian A. Ryan, Barbra Cathcart, et al. "An unusual case of a giant fetal facial tumour and review of the literature." Irish Journal of Medical Science (1971 -), March 25, 2023. http://dx.doi.org/10.1007/s11845-023-03344-3.

Full text

Abstract:

Abstract We present the case of a pregnant 32-year-old woman who presented with a giant fetal facial tumour at 22 weeks. The mass, initially 4 × 3.5 × 3 cm in size, was largely cystic with a small solid component. It subsequently increased to 9 × 9 × 10 cm. Significant compression effects on the fetal orbit, temple and infratemporal fossa, with potential compression of the optic nerve, were noted on ultrasound and MRI. The cyst required drainage twice in the pregnancy: firstly to reduce the compression effects and secondly to facilitate caesarean delivery. Postnatally, the baby had significant

APA, Harvard, Vancouver, ISO, and other styles

41

Yamasaki, Yui, Yoshiya Miyahara, Hiroki Morita, Ichiro Morioka, Yasuhiko Ebina, and Hideto Yamada. "A case of congenital brain teratoma extending into the orbit." Case Reports in Perinatal Medicine 4, no. 1 (2015). http://dx.doi.org/10.1515/crpm-2014-0027.

Full text

Abstract:

AbstractCongenital tumors arising from the central nervous system are uncommon. A 31-year-old pregnant woman had an uneventful course until 33 weeks of gestation (GW). An ultrasonographic examination at 35 GW first demonstrated an increase in fetal head size. The brain midline shifted to the left side due to the intracranial tumor extending into the orbit in the right hemisphere at 36 GW. The brain teratoma in the fetus was suspected by magnetic resonance imaging of the heterogeneous enhancement and calcification. The male baby was delivered by cesarean section at 36 GW and he had facial dimor

APA, Harvard, Vancouver, ISO, and other styles

42

Imbelloni, Luiz Eduardo. "Cranio Cervico Facial Oral Teratoma in a 32-Day-Old Infant with Intrauterine Diagnosis." Biomedical Journal of Scientific & Technical Research 59, no. 3 (2024). https://doi.org/10.26717/bjstr.2024.59.009300.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Yao, Haifeng, Zhaoxin Li, Zhaohui Zhai, and Yuli Li. "Primary benign mature teratoma of facial fronto-temporal region in adolescent: A case report." Asian Journal of Surgery, December 2022. http://dx.doi.org/10.1016/j.asjsur.2022.11.101.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Arumugham, Dharmeshwar, Jayachandran Sadaksharam, and Vidya Jayaram. "Case of congenital mandibular malformation: A rarity." Annals of the National Academy of Medical Sciences (India), March 8, 2025, 1–4. https://doi.org/10.25259/anams_20_2024.

Full text

Abstract:

The condition known as craniofacial duplication, or Diprosopus, is an exceedingly rare occurrence. The term “Diprosopus” originates from Greek, meaning “two-faced person.” This condition can involve a wide range of anomalies, from complete duplication of facial features to partial duplication of specific facial structures. It is a congenital developmental abnormality typically identified during prenatal development or in the early stages of a child’s growth. Formerly, it was believed to be an anomaly rather than a teratoma. The first documented report of this unique phenomenon was by Mclaughli

APA, Harvard, Vancouver, ISO, and other styles

45

Robilliard, R., G. Tung, K. Svokos, R. Lulla, and J. Q. Quintos. "7202 CPP with Rapid Pubertal Progression in a 9-Year-Old Boy with Hypothalamic Teratoma." Journal of the Endocrine Society 8, Supplement_1 (2024). http://dx.doi.org/10.1210/jendso/bvae163.1425.

Full text

Abstract:

Abstract Disclosure: R. Robilliard: None. G. Tung: None. K. Svokos: None. R. Lulla: None. J.Q. Quintos: None. Background: Central Precocious Puberty (CPP) in males is rare, with incidence of 0.01-2/10,000. The most common identifiable cause of CPP in young children is hypothalamic hamartoma. No case hypothalamic teratoma has been reported to cause CPP in males. Clinical Case: At the age of 10-years and 5-months, a boy presented to the pediatric endocrinology with signs of precocious puberty including facial hair development, voice deepening, and increased growth velocity that began at 9 years

APA, Harvard, Vancouver, ISO, and other styles

46

Montoro-Membila, Nuria, Angel Gómez-Camello, Inmaculada Villegas-Rodríguez, and Mónica Triviño-Mosquera. "Cognitive profile in anti-NMDAR encephalitis: Neuropsychological evaluation, rehabilitation, and evolution. A case report." Neuropsychologie clinique et appliquée 4, Spring 2021 (2021). http://dx.doi.org/10.46278/j.ncacn20210429.

Full text

Abstract:

Encephalitis associated with antibodies against the N-methyl-D-aspartate receptor (i.e., anti-NMDAR encephalitis) is an immune-mediated disorder mainly affecting girls and young women with ovarian teratoma. The clinical picture of the disease progresses from headaches and seizures, psychopathological symptoms (i.e., anxiety, psychosis, or hyperreligiosity), and neuropsychological deficits (i.e., memory, attention, and language disintegration) into a state of agitation, catatonia, dysautonomia (i.e., abnormal movements due to inappropriate muscular activity) and facial dyskinesia. Reports of th

APA, Harvard, Vancouver, ISO, and other styles

47

Rattan, Kamal N., and Bikramjeet Singh. "Tessier 30 Facial Cleft- Median Cleft of Upper and Lower Lip, Lower Alveolus and Mandible, Ankyloglossia and Cervical Teratoma." otolaryngology 6, no. 4 (2016). http://dx.doi.org/10.4172/2161-119x.1000247.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Prezioso, Giovanni, Maddalena Petraroli, Michela Bergonzani, et al. "Duplication of the Pituitary Gland (DPG)-Plus Syndrome Associated With Midline Anomalies and Precocious Puberty: A Case Report and Review of the Literature." Frontiers in Endocrinology 12 (May 26, 2021). http://dx.doi.org/10.3389/fendo.2021.685888.

Full text

Abstract:

Duplication of the pituitary gland (DPG)-plus syndrome is a very rare developmental disorder with few cases described in the literature and characterized by multiple midline and central nervous system malformations. The hypothalamus and hypophysis involvement may be clinically associated with endocrine abnormalities. A 5.9-year-old female child was admitted to our Clinic for premature thelarche and acceleration of growth. DPG-plus syndrome with paired infundibula and pituitary glands was diagnosed after birth, when she appeared small for gestational age and she presented with lingual hypoplasi

APA, Harvard, Vancouver, ISO, and other styles

49

Chen, Han, Cai-Yan Mo, and Li-yong Zhong. "Central precocious puberty secondary to peripheral precocious puberty due to a pineal germ cell tumor: a case and review of literature." BMC Endocrine Disorders 23, no. 1 (2023). http://dx.doi.org/10.1186/s12902-023-01494-0.

Full text

Abstract:

Abstract Background The pineal lesion affecting melatonin is a rare cause of central precocious puberty by decreasing the inhibition of hypothalamic–pituitary–gonadal axis. Germ cell tumor secreting human chorionic gonadotropin is a rare cause of peripheral puberty. Case presentation A 5.8-year-old male presented facial hair and phallic growth, deepened voice, and accelerated growth velocity for 6 months. The elevated human chorionic gonadotropin level with undetectable gonadotropin levels indicated peripheral precocious puberty. Brain imaging revealed a pineal mass and further pathology indic

APA, Harvard, Vancouver, ISO, and other styles

50

Xie, Zhengxing, Yan Zhuang, and Jieping Liu. "Fully endoscopic neurosurgery using a two-handed technique for cerebellopontine angle tumors via the retrosigmoid approach." Frontiers in Oncology 14 (December 16, 2024). https://doi.org/10.3389/fonc.2024.1485932.

Full text

Abstract:

BackgroundSurgery for tumors in the cerebellopontine angle is always a significant challenge due to the densely packed neurovascular structures, the narrow deep location, and the complex relationship between the lesions and surrounding neurovascular structures. Recently, great attention has been given to the neuroendoscope for its exclusive advantages, which have added a new dimension to many classical microscopic surgeries. However, the feasibility and advisability of fully endoscopic neurosurgery for cerebellopontine angle tumors remain to be further evaluated.MethodsWe retrospectively colle

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!