Fetal axillary cystic hygroma: A novel association with triple X syndrome

İskender, Cantekin; Tarım, Ebru; Çok, Tayfun; Yalçınkaya, Cem; Kalaycı, Hakan; Şahin, Feride İffet

doi:10.1002/bdra.23083

Cited by 7 publications

(4 citation statements)

References 11 publications

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“…We searched PubMed, Scopus, and the Web of Science for all consecutive cases of fetal axillary cystic hygroma or lymphangioma as well as hemangiolymphangioma. Up to May 2017, 25 cases of axillary lymphangioma were published, as presented in Table . The review included only cystic hygromas and lymphangiomas mainly located at the axilla, but they might extend to the chest wall, the neck, or even the thorax.…”

Section: Literature Review and Analysismentioning

confidence: 99%

“…Up to May 2017, 25 cases of axillary lymphangioma were published, as presented in Table 1. [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20] The review included only cystic hygromas and lymphangiomas mainly located at the axilla, but they might extend to the chest wall, the neck, or even the thorax. Together with 5 our own cases, a total of 30 cases were analyzed and summarized as follows: be taken into account for decisions on the route of delivery.…”

Section: Literature Review and Analysismentioning

confidence: 99%

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Natural Course of Fetal Axillary Lymphangioma Based on Prenatal Ultrasound Studies

Tongsong

Luewan

Khorana

et al. 2017

J of Ultrasound Medicine

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This series and literature review aimed to prenatally characterize the nature of axillary lymphangioma. A total of 30 cases, including our 5 cases, were analyzed. Insights gained from this review are as follows: Septate and nonseptate cysts seem to be different entities. The nonseptate type tends to be small and transient but more highly associated with aneuploidies. Septate cysts are very rarely associated with other abnormalities and hydrops fetalis, unlike cystic hygroma colli, but are more progressive with gestational age and associated with adverse outcomes. The cases with high flow have a higher risk of intralesional hemorrhage. Prenatal diagnosis is important for the route of timely delivery and possibly prenatal interventions. Shoulder dystocia is common and should always be taken into account for decisions on the route of delivery.

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Section: Literature Review and Analysismentioning

confidence: 99%

Section: Literature Review and Analysismentioning

confidence: 99%

Natural Course of Fetal Axillary Lymphangioma Based on Prenatal Ultrasound Studies

Tongsong

Luewan

Khorana

et al. 2017

J of Ultrasound Medicine

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“…There was no written lay information on Triple X, yet Kate's university had a medical school and therefore she had unique and full access to medical journal articles. But these medical articles were narrowly focused, somewhat dehumanising, and focused on failure (see [11][12][13]).…”

Section: Authors' Backgroundsmentioning

confidence: 99%

Notes from the Field of the Scholar–Practitioner: Inhabiting the Liminal Space between Research and Practice—A Reflective Account of Holding Dual Identities

Stevens-Wood,

Attfield

2024

Societies

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Kirsten and Kate are scholar–practitioners studying the people with whom they interact and operate. In this empirical paper, based on their auto/ethnographic reflections, they study some often-neglected circumstances and by-products of scholar–practitioner research. They review aspects of entering research situations with which they are connected, participating in them, leaving them behind, and revisiting them. Kirsten is an ethnographer, both working with and studying intentional communities. Kate is a qualitative researcher who operates auto/ethnographically in studying Triple X unintentional communities. This article arises from discussions of Kirsten’s and Kate’s field notes, which have led them to compare and relate their convergent experiences with one another. Kirsten and Kate focus on the physical culture of the environments in which they study. Some traditional boundaries like the isolation of researchers and communities are eroding. Kirsten and Kate care about those they study and continue to hold some responsibility for the lives of people they have entered. They attempt to narrow the space between theory and practice in recognising their interconnected nature. Civic mission is gaining increased currency for researchers and may form a signpost towards the future of research.

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“…Given the frequency of TXS in the general population, the low number of reports of neoplasms in this syndrome is at least notable. The few publications on TXS and neoplasms so far are case reports and concede that it might be a chance or coincidence (12)(13)(14)(15)(16) or consider the potential influence of mosaic or constitutional TXS status on immunological therapies (17)(18).…”

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confidence: 99%

Symptomatic Mandibular Fibrous Dysplasia With Concurrent Triple X- and Premutation Stage Fragile-X-Syndrome: Case Report With Short Literature Survey

2019

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Background: Certain constitutive chromosomal abnormalities of the human X chromosome are relatively common in conspicuous neuropsychiatric findings. Although tumors or tumor-like lesions are occasionally reported in diseases of the X chromosome, they are numerically negligible, for example, in aneuploidy such as the triple X syndrome (TXS). Case Report: A 16-year-old female patient with a known TXS and premutation stage of fragile X syndrome was referred by her dentist for diagnosis and treatment of unilateral cheek swelling. The examination of the psychologically conspicuous patient revealed a unilateral mandibular tumor with dysesthesia of the mental nerve. Surgical removal of soft, crumbly spongiosa over the nerve canal resulted in sufficient pressure release of the constricted nerve and restoration of epicritic sensitivity. Imaging findings and histological and molecular genetic examination revealed monostotic craniofacial fibrous dysplasia. Conclusion: Although the data in the literature do not give reason to suppose an accumulation of neoplasms in TXS, a numb chin syndrome should be a reason for detailed diagnostics. Careful diagnosis allows for customized therapy. This is the first report on the coincidence of TXS, fragile X syndrome, and fibrous dysplasia in a single individual.

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Fetal axillary cystic hygroma: A novel association with triple X syndrome

Abstract: This is a novel description of axillary CH associated with triple X syndrome.

Cited by 7 publications

References 11 publications

Natural Course of Fetal Axillary Lymphangioma Based on Prenatal Ultrasound Studies

Natural Course of Fetal Axillary Lymphangioma Based on Prenatal Ultrasound Studies

Notes from the Field of the Scholar–Practitioner: Inhabiting the Liminal Space between Research and Practice—A Reflective Account of Holding Dual Identities

Symptomatic Mandibular Fibrous Dysplasia With Concurrent Triple X- and Premutation Stage Fragile-X-Syndrome: Case Report With Short Literature Survey

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