Familial hypocalciuric hypercalcemia surgery: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Familial hypocalciuric hypercalcemia}} | {{Familial hypocalciuric hypercalcemia}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}} {{Ajay}} | ||
==Overview== | ==Overview== | ||
Surgical intervention is not recommended for the management of | Surgical intervention is not recommended for the management of [[familial hypocalciuric hypercalcemia]]. Very rarely its done in patients with associated [[pancreatitis]], [[parathyroid adenoma]], [[hyperparathyroidism]], and hypercalciuria. | ||
==Surgery== | ==Surgery== | ||
*Surgical intervention is not recommended for the management of FHH. | *Surgical intervention is not recommended for the management of [[Familial hypocalciuric hypercalcemia|FHH]]. | ||
==Indications== | ===Indications=== | ||
Parathyroidectomy in FHH is rarely done in patients if associated conditions are present along with the FHH such as<ref name="pmid19423559">{{cite journal |vauthors=Brachet C, Boros E, Tenoutasse S, Lissens W, Andry G, Martin P, Bergmann P, Heinrichs C |title=Association of parathyroid adenoma and familial hypocalciuric hypercalcaemia in a teenager |journal=Eur. J. Endocrinol. |volume=161 |issue=1 |pages=207–10 |year=2009 |pmid=19423559 |doi=10.1530/EJE-09-0257 |url=}}</ref><ref name="pmid10843194">{{cite journal |vauthors=Carling T, Szabo E, Bai M, Ridefelt P, Westin G, Gustavsson P, Trivedi S, Hellman P, Brown EM, Dahl N, Rastad J |title=Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor |journal=J. Clin. Endocrinol. Metab. |volume=85 |issue=5 |pages=2042–7 |year=2000 |pmid=10843194 |doi=10.1210/jcem.85.5.6477 |url=}}</ref> | [[Parathyroidectomy]] in FHH is rarely done in patients if associated conditions are present along with the [[Familial hypocalciuric hypercalcemia|FHH]] such as<ref name="pmid19423559">{{cite journal |vauthors=Brachet C, Boros E, Tenoutasse S, Lissens W, Andry G, Martin P, Bergmann P, Heinrichs C |title=Association of parathyroid adenoma and familial hypocalciuric hypercalcaemia in a teenager |journal=Eur. J. Endocrinol. |volume=161 |issue=1 |pages=207–10 |year=2009 |pmid=19423559 |doi=10.1530/EJE-09-0257 |url=}}</ref><ref name="pmid10843194">{{cite journal |vauthors=Carling T, Szabo E, Bai M, Ridefelt P, Westin G, Gustavsson P, Trivedi S, Hellman P, Brown EM, Dahl N, Rastad J |title=Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor |journal=J. Clin. Endocrinol. Metab. |volume=85 |issue=5 |pages=2042–7 |year=2000 |pmid=10843194 |doi=10.1210/jcem.85.5.6477 |url=}}</ref> | ||
Parathyroid adenoma | * [[Parathyroid adenoma]] | ||
Pancreatitis | |||
Hyperparathyroidism | * [[Pancreatitis]] | ||
Hypercalciuria | |||
* [[Hyperparathyroidism]] | |||
* Hypercalciuria | |||
==References== | ==References== | ||
Latest revision as of 18:32, 2 October 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ajay Gade MD[2]]
Overview
Surgical intervention is not recommended for the management of familial hypocalciuric hypercalcemia. Very rarely its done in patients with associated pancreatitis, parathyroid adenoma, hyperparathyroidism, and hypercalciuria.
Surgery
- Surgical intervention is not recommended for the management of FHH.
Indications
Parathyroidectomy in FHH is rarely done in patients if associated conditions are present along with the FHH such as[1][2]
- Hypercalciuria
References
- ↑ Brachet C, Boros E, Tenoutasse S, Lissens W, Andry G, Martin P, Bergmann P, Heinrichs C (2009). "Association of parathyroid adenoma and familial hypocalciuric hypercalcaemia in a teenager". Eur. J. Endocrinol. 161 (1): 207–10. doi:10.1530/EJE-09-0257. PMID 19423559.
- ↑ Carling T, Szabo E, Bai M, Ridefelt P, Westin G, Gustavsson P, Trivedi S, Hellman P, Brown EM, Dahl N, Rastad J (2000). "Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor". J. Clin. Endocrinol. Metab. 85 (5): 2042–7. doi:10.1210/jcem.85.5.6477. PMID 10843194.