Dilemma in primary hyperparathyroidism with multiple brown tumors
Primary hyperparathyroidism (PHPT) is a disease characterized by excessive secretion of parathormone. During the disease, bone loss occurs, particularly depending on the resorption of the skeletal system. One of the complications of PHPT is fibrotic, cystic bony changes which are called a brown tumo...
Ausführliche Beschreibung
Autor*in: |
Girish Mysore Suresh [verfasserIn] Ravi Arjunan [verfasserIn] S Altaf [verfasserIn] Veerendra Kumar [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2020 |
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Übergeordnetes Werk: |
In: Formosan Journal of Surgery - Wolters Kluwer Medknow Publications, 2017, 53(2020), 1, Seite 35-38 |
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Übergeordnetes Werk: |
volume:53 ; year:2020 ; number:1 ; pages:35-38 |
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DOI / URN: |
10.4103/fjs.fjs_45_19 |
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DOAJ078105048 |
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10.4103/fjs.fjs_45_19 doi (DE-627)DOAJ078105048 (DE-599)DOAJ7931300bcef7440d8f90f5e14f54fd67 DE-627 ger DE-627 rakwb eng RD1-811 Girish Mysore Suresh verfasserin aut Dilemma in primary hyperparathyroidism with multiple brown tumors 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Primary hyperparathyroidism (PHPT) is a disease characterized by excessive secretion of parathormone. During the disease, bone loss occurs, particularly depending on the resorption of the skeletal system. One of the complications of PHPT is fibrotic, cystic bony changes which are called a brown tumor (BT). Skeletal manifestations in the form of BTs are rare, and according to literature studies, it occurs in <2% of patients suffering from any form of HPT. As it is a rare disease and multiple benign lesions may simulate a malignant neoplasm and pose a real challenge for the clinician in its differential diagnosis. We present the case of a 35-year-old man who was evaluated for multiple lytic expansile lesions with a strong suspicion of malignancy and fibrous dysplasia but turned out to be a case of PHPT. brown tumors parathyroid adenoma primary hyperparathyroidism Surgery Ravi Arjunan verfasserin aut S Altaf verfasserin aut Veerendra Kumar verfasserin aut In Formosan Journal of Surgery Wolters Kluwer Medknow Publications, 2017 53(2020), 1, Seite 35-38 (DE-627)683365509 (DE-600)2645317-4 22135413 nnns volume:53 year:2020 number:1 pages:35-38 https://doi.org/10.4103/fjs.fjs_45_19 kostenfrei https://doaj.org/article/7931300bcef7440d8f90f5e14f54fd67 kostenfrei http://www.e-fjs.org/article.asp?issn=1682-606X;year=2020;volume=53;issue=1;spage=35;epage=38;aulast= kostenfrei https://doaj.org/toc/1682-606X Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_100 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2055 GBV_ILN_2111 AR 53 2020 1 35-38 |
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Primary hyperparathyroidism (PHPT) is a disease characterized by excessive secretion of parathormone. During the disease, bone loss occurs, particularly depending on the resorption of the skeletal system. One of the complications of PHPT is fibrotic, cystic bony changes which are called a brown tumor (BT). Skeletal manifestations in the form of BTs are rare, and according to literature studies, it occurs in <2% of patients suffering from any form of HPT. As it is a rare disease and multiple benign lesions may simulate a malignant neoplasm and pose a real challenge for the clinician in its differential diagnosis. We present the case of a 35-year-old man who was evaluated for multiple lytic expansile lesions with a strong suspicion of malignancy and fibrous dysplasia but turned out to be a case of PHPT. |
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Primary hyperparathyroidism (PHPT) is a disease characterized by excessive secretion of parathormone. During the disease, bone loss occurs, particularly depending on the resorption of the skeletal system. One of the complications of PHPT is fibrotic, cystic bony changes which are called a brown tumor (BT). Skeletal manifestations in the form of BTs are rare, and according to literature studies, it occurs in <2% of patients suffering from any form of HPT. As it is a rare disease and multiple benign lesions may simulate a malignant neoplasm and pose a real challenge for the clinician in its differential diagnosis. We present the case of a 35-year-old man who was evaluated for multiple lytic expansile lesions with a strong suspicion of malignancy and fibrous dysplasia but turned out to be a case of PHPT. |
abstract_unstemmed |
Primary hyperparathyroidism (PHPT) is a disease characterized by excessive secretion of parathormone. During the disease, bone loss occurs, particularly depending on the resorption of the skeletal system. One of the complications of PHPT is fibrotic, cystic bony changes which are called a brown tumor (BT). Skeletal manifestations in the form of BTs are rare, and according to literature studies, it occurs in <2% of patients suffering from any form of HPT. As it is a rare disease and multiple benign lesions may simulate a malignant neoplasm and pose a real challenge for the clinician in its differential diagnosis. We present the case of a 35-year-old man who was evaluated for multiple lytic expansile lesions with a strong suspicion of malignancy and fibrous dysplasia but turned out to be a case of PHPT. |
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title_short |
Dilemma in primary hyperparathyroidism with multiple brown tumors |
url |
https://doi.org/10.4103/fjs.fjs_45_19 https://doaj.org/article/7931300bcef7440d8f90f5e14f54fd67 http://www.e-fjs.org/article.asp?issn=1682-606X;year=2020;volume=53;issue=1;spage=35;epage=38;aulast= https://doaj.org/toc/1682-606X |
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Ravi Arjunan S Altaf Veerendra Kumar |
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2024-07-03T15:58:53.723Z |
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