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This study described a case of plurihormonal tumor associated with papillary thyroid carcinoma (PTC) and summarized the treatment approaches for similar cases, while also exploring the underlying pathogenesis. The patient exhibited symptoms indicative of acromegaly, central hyperthyroidism, and hyperprolactinemia. A glucose loading test demonstrated persistently elevated growth hormone (GH) levels, while thyroid function tests revealed inappropriate thyroid stimulating hormone (TSH) secretion. Imaging of the pituitary gland revealed a 26 × 19 mm lesion compressing the optic chiasm. Thyroid ultrasound reveals bilateral Thyroid Imaging Reporting and Data System 4B nodules, with the largest on the right measuring 27 × 20 mm. Fine-needle aspiration cytology (FNAC) revealed the presence of PTC. Three weeks later, the patient underwent pituitary adenomectomy. Immunohistochemistry revealed a plurihormonal tumor positive for TSH, GH, luteinizing hormone (LH), prolactin (PRL), pituitary-specific transcription factor 1 (Pit1), and steroidogenic factor 1 (SF1). A total thyroidectomy followed 10 weeks post-adenomectomy. Immunohistochemical evaluation showed higher nuclear positivity for the high-mobility group AT-hook 1 (HMGA1) and the high-mobility group AT-hook 2 (HMGA2) proteins in neoplastic cells compared to normal tissues. In our search results, only three similar cases were identified, and we summarized the relevant literature search results which raise the possibility that the HMGA2-the Retinoblastoma Protein (pRB)/E2F Transcription Factor 1 (E2F1)-HMGA1 signaling pathway may represent a common pathogenic pathway for PTC and plurihormonal tumor. If a patient simultaneously suffers from PTC and plurihormonal tumor, the determination of the surgical sequence is crucial. In cases of postoperative recurrence, where patients are reluctant to undergo additional surgeries, targeting HMGA is likely to offer a promising approach to prevent the progression of both the pituitary tumors and PTC.
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http://dx.doi.org/10.1111/neup.70005 | DOI Listing |
Cells
July 2025
Department of Microscopic Morphology/Histology, "Victor Babes" University of Medicine and Pharmacy, 300041 Timisoara, Romania.
Pituitary neuroendocrine tumors (PitNETs) represent a complex pathology based on numerous incompletely elucidated molecular mechanisms. Beyond tumor cells, analyzing the tumor microenvironment may help identify novel prognostic markers and therapies. A key component of this environment is the folliculo-stellate (FS) cell.
View Article and Find Full Text PDFPlurihormonal pituitary neuroendocrine tumors/pituitary adenomas (PitNET/PAs) express multiple hormones and/or transcription factors. The two most common subtypes within the plurihormonal category are immature PIT-1 (pituitary-specific POU-class homeodomain factor-1) lineage tumors and mature PIT-1 plurihormonal tumors, most of which show PIT-1/SF-1 (steroidogenic factor 1) co-expression. Our aim is to provide direct comparison between these two PIT-1 plurihormonal tumor types in terms of demographic, radiological, neurosurgical, and endocrinological features.
View Article and Find Full Text PDFActa Neuropathol Commun
June 2025
Department of Neuropathology, University Hospital Tübingen, Eberhard-Karls-University Tübingen, 72076, Tübingen, Germany.
The WHO classifications of 2017 and 2022 recommend the use of pituitary transcription factors PIT-1, T-PIT and SF-1 as well as GATA3 and ERα for histopathological diagnosis. The aim of this study is to demonstrate their diagnostic impact in a large retrospective cohort. 921 PitNETs/PAs diagnosed in our department between October 2004 and April 2018 were retrospectively reassessed according to the WHO classifications 2017 and 2022.
View Article and Find Full Text PDFEndocr Pathol
June 2025
Department of Pathology, Institute of Pathology, University Hospitals Cleveland, Case Western Reserve University, 11100 Euclid AvenueRoom 212, Cleveland, OH, 44106, USA.
We studied transcription factors and hormones expressed by duodenal neuroendocrine cells in a consecutively diagnosed series of 53 patients with well-differentiated duodenal NETs. There were 30 men; the mean age was 65 years (33 to 81). The study included biopsies (n = 18), endoscopic mucosal resections (n = 19), and surgical resections (n = 16).
View Article and Find Full Text PDFJ Vet Intern Med
June 2025
Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, the Netherlands.
A 12-year-old, male Labrador Retriever was presented because of polyuria, polydipsia, polyphagia, joint pain, and physical features consistent with acromegaly. Circulating insulin-like growth factor-1 (IGF-1) concentration was increased (> 1000 ng/mL; reference interval [RI], 42-449), suggestive of hypersomatotropism. An abnormal low-dose dexamethasone suppression test and increased circulating adrenocorticotropic (ACTH) concentration indicated pituitary-dependent hypercortisolism.
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