Selected Topics in the Pathology of the Thyroid and Parathyroid Glands in Children and Adolescents

Ozolek, John A.

doi:10.1007/s12105-020-01274-5

Cited by 5 publications

(6 citation statements)

References 106 publications

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“…Cribriform morular thyroid carcinoma is an entity independent from PTC and is classically ETA Guidelines Pediatric Thyroid Nodules and DTC September 2022 | Version 8.2 12 associated with familial adenomatous polyposis but also occurs due to somatic mutations [46]. The prognosis of cribriform morular thyroid carcinoma is good, mainly because these tumors tend to be encapsulated/well circumscribed [47].…”

Section: B4 Histopathologic Characteristics Of Dtcmentioning

confidence: 99%

2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma

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Czarniecka

et al. 2022

European Thyroid Journal

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At present no European recommendations for the management of pediatric thyroid nodules and differentiated thyroid carcinoma (DTC) exist. Differences in clinical, molecular, and pathological characteristics between pediatric and adult DTC emphasize the need for specific recommendations for the pediatric population. An expert panel was instituted by the executive committee of the European Thyroid Association (ETA) including an international community of experts from a variety of disciplines including pediatric and adult endocrinology, pathology, endocrine surgery, nuclear medicine, clinical genetics, and oncology. The American Thyroid Association (ATA) pediatric guideline 2015 was used as framework for the present guideline. Areas of discordance were identified, and clinical questions were formulated. The expert panel members discussed the evidence and formulated recommendations based upon the latest evidence and expert opinion. Children with a thyroid nodule or DTC require expert care in an experienced center. The present guideline provides guidance for healthcare professionals to make well-considered decisions together with patients and parents regarding diagnostics, treatment and follow-up of pediatric thyroid nodules and DTC.

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Section: B4 Histopathologic Characteristics Of Dtcmentioning

confidence: 99%

2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma

Lebbink

Links

Czarniecka

et al. 2022

European Thyroid Journal

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“…Cribriform-morular thyroid carcinoma is an entity independent from PTC and is classically associated with familial adenomatous polyposis and also occurs due to somatic mutations (47). The prognosis of cribriform-morular thyroid carcinoma is good, mainly because these tumors tend to be encapsulated/wellcircumscribed (48). Follicular thyroid carcinoma (is very rare during childhood and is usually minimally invasive (49).…”

Section: B4 Histopathologic Characteristics Of Dtcmentioning

confidence: 99%

2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma

CA,

TP,

et al. 2023

ESPE

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At present, no European recommendations for the management of pediatric thyroid nodules and differentiated thyroid carcinoma (DTC) exist. Differences in clinical, molecular, and pathological characteristics between pediatric and adult DTC emphasize the need for specific recommendations for the pediatric population. An expert panel was instituted by the executive committee of the European Thyroid Association including an international community of experts from a variety of disciplines including pediatric and adult endocrinology, pathology, endocrine surgery, nuclear medicine, clinical genetics, and oncology. The 2015 American Thyroid Association Pediatric Guideline was used as framework for the present guideline. Areas of discordance were identified, and clinical questions were formulated. The expert panel members discussed the evidence and formulated recommendations based on the latest evidence and expert opinion. Children with a thyroid nodule or DTC require expert care in an experienced center. The present guideline provides guidance for healthcare professionals to make well-considered decisions together with patients and parents regarding diagnosis, treatment, and follow-up of pediatric thyroid nodules and DTC. Keywords f pediatric f thyroid cancer f thyroid nodule f recommendation f European

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“…Four of 5 patients had only meningioma and thyroid neoplasia as manifestation of their multiple tumors. Gardner/Turcot syndrome (APC-associated polyposis), PTEN hamartoma syndrome (Cowden, Bannayan-Riley-Ruvalcaba, Lhermitte-Duclos syndromes), MEN1 (Wermer syndrome), and Werner syndrome are familial inherited syndromes also highly associated with thyroid neoplasia [67]. Carney complex also has a high Meninges Outside the Meninges: Ectopic Meningiomas and Meningothlelial Proliferations DOI: http://dx.doi.org/10.5772/intechopen.100206 association of thyroid neoplasia and has as a pathognomonic lesion the melanotic schwannoma, a tumor characterized by schwannian differentiation with the feature of psammoma bodies.…”

Section: Meningothelial Meningioma Of the Mastoid Presenting With Tinnitus In A 46-year-old Woman No Connection To The Cns Was Seen By Immentioning

confidence: 99%

“…Carney complex also has a high Meninges Outside the Meninges: Ectopic Meningiomas and Meningothlelial Proliferations DOI: http://dx.doi.org/10.5772/intechopen.100206 association of thyroid neoplasia and has as a pathognomonic lesion the melanotic schwannoma, a tumor characterized by schwannian differentiation with the feature of psammoma bodies. Carney complex is known to result from mutations in PRKAR1A (chromosome 17q22-24) and CNC2 (2p16) while WHO grades II and III meningiomas have been shown to be associated with gains and amplification of 17q [53,54,67]. In addition, interestingly, Gardner/Turcot syndrome, Carney complex, and Werner syndrome all have various bone tumors as part of the manifestation/ diagnostic criteria for their respective syndromes.…”

Section: Meningothelial Meningioma Of the Mastoid Presenting With Tinnitus In A 46-year-old Woman No Connection To The Cns Was Seen By Immentioning

confidence: 99%

Meninges Outside the Meninges: Ectopic Meningiomas and Meningothlelial Proliferations

Ozolek¹

2022

Brain Tumors

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Extracranial meningiomas have been reported for decades now and have been described in the head and neck; calvarial, nasal cavity, paranasal sinuses, nasopharynx, parotid gland and in various remote anatomical locations systemically. The presence of microanatomical structures for all intents and purposes resembling and having the histopathological characteristics of meninges outside of the central nervous system meninges is uncommon but well-documented. Typically, these lesions are found in the lung or part of hamartomatous/choristomatous lesions and frequently occur in the head and neck anatomical region. The lesion first described by Suster and Rosai termed \"hamartoma of the scalp with ectopic meningothelial elements\" is the prototypical example of lesions with meningothelial elements. We have described recently a similar hamartomatous lesion with meningothelial elements occurring in the tongue. In this chapter, we will review the clinicopathological features of ectopic meningiomas and lesions that contain meningothelial elements and their possible pathogenesis.

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Selected Topics in the Pathology of the Thyroid and Parathyroid Glands in Children and Adolescents

Cited by 5 publications

References 106 publications

2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma

2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma

2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma

Meninges Outside the Meninges: Ectopic Meningiomas and Meningothlelial Proliferations

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