213
Views
2
CrossRef citations to date
0
Altmetric
CASE REPORT

A Complete Form of Pachydermoperiostosis Accompanied by a Pituitary Microadenoma

ORCID Icon &
Pages 47-52 | Received 13 Sep 2022, Accepted 30 Dec 2022, Published online: 06 Jan 2023

References

  • Xiao J, Zhang DD, Zhang L. A novel mutation in the SLCO2A1 gene in a Chinese family with pachydermoperiostosis. Australas J Dermatol. 2019;60(4):e348–e350. doi:10.1111/ajd.13041
  • Honório MLP, Bezerra GH, Costa V. Complete form of pachydermoperiostosis. An Bras Dermatol. 2020;95(1):98–101. doi:10.1016/j.abd.2019.04.009
  • Prasad A, Shahi P, Sehgal A, Bhagirathi Mallikarjunaswamy M. Incomplete primary hypertrophic osteoarthropathy. BMJ Case Rep. 2020;13(5):e236034. doi:10.1136/bcr-2020-236034
  • Mehta GU, Lonser RR. Management of hormone-secreting pituitary adenomas. Neuro Oncol. 2017;19(6):762–773. doi:10.1093/neuonc/now130
  • Ezzat S, Asa SL, Couldwell WT, et al. The prevalence of pituitary adenomas: a systematic review. Cancer. 2004;101(3):613–619. doi:10.1002/cncr.20412
  • Ntali G, Wass JA. Epidemiology, clinical presentation and diagnosis of non-functioning pituitary adenomas. Pituitary. 2018;21(2):111–118. doi:10.1007/s11102-018-0869-3
  • Lim CT, Korbonits M. Update On The Clinicopathology Of Pituitary Adenomas. Endocr Pract. 2018;24(5):473–488. doi:10.4158/ep-2018-0034
  • Shimizu C, Kubo M, Kijima H, et al. A rare case of acromegaly associated with pachydermoperiostosis. J Endocrinol Invest. 1999;22(5):386–389. doi:10.1007/bf03343577
  • Berdia J, Tsai FF, Liang J, Shinder R. Pachydermoperiostosis: a rare cause of marked blepharoptosis and floppy eyelid syndrome. Orbit. 2013;32(4):266–269. doi:10.3109/01676830.2013.788672
  • Yap FY, Skalski MR, Patel DB, et al. Hypertrophic Osteoarthropathy: clinical and Imaging Features. Radiographics. 2017;37(1):157–195. doi:10.1148/rg.2017160052
  • Abdullah NRA, Jason WLC, Nasruddin AB. Pachydermoperiostosis: a rare mimicker of acromegaly. Endocrinol Diabetes Metab Case Rep. 2017;2017. doi:10.1530/edm-17-0029
  • Cheng SK, Michael A, Rizzuti AE. Pachydermoperiostosis presenting with vision loss secondary to severe phlyctenular keratoconjunctivitis. Cornea. 2022;41(1):113–115. doi:10.1097/ico.0000000000002700
  • Wang Q, Li YH, Lin GL, et al. Primary hypertrophic osteoarthropathy related Gastrointestinal complication has distinctive clinical and pathological characteristics: two cases report and review of the literature. Orphanet J Rare Dis. 2019;14(1):297. doi:10.1186/s13023-019-1264-5
  • Vilar L, Vilar CF, Lyra R, Lyra R, Naves LA. Acromegaly: clinical features at diagnosis. Pituitary. 2017;20(1):22–32. doi:10.1007/s11102-016-0772-8
  • Kartal Baykan E, Türkyılmaz A. Differential diagnosis of acromegaly: pachydermoperiostosis two new cases from Turkey. J Clin Res Pediatr Endocrinol. 2022;14(3):350–355. doi:10.4274/jcrpe.galenos.2021.2020.0301
  • Katznelson L, Laws ER, Melmed S, et al. Acromegaly: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2014;99(11):3933–3951. doi:10.1210/jc.2014-2700
  • Jadidi J, Sigari M, Efendizade A, Grigorian A, Lehto SA, Kolla S. Thyroid acropachy: a rare skeletal manifestation of autoimmune thyroid disease. Radiol Case Rep. 2019;14(8):917–919. doi:10.1016/j.radcr.2019.04.021
  • Fatourechi V, Ahmed DD, Schwartz KM. Thyroid acropachy: report of 40 patients treated at a single institution in a 26-year period. J Clin Endocrinol Metab. 2002;87(12):5435–5441. doi:10.1210/jc.2002-020746
  • Perini N, Santos RB, Romaldini JH, Villagelin D. Thyroid acropachy: a rare manifestation of graves disease in joints. AACE Clin Case Rep. 2019;5(6):e369–e371. doi:10.4158/accr-2018-0591
  • Aimaretti G, Boschetti M, Corneli G, et al. Normal age-dependent values of serum insulin growth factor-I: results from a healthy Italian population. J Endocrinol Invest. 2008;31(5):445–449. doi:10.1007/bf03346389
  • Kato Y, Murakami Y, Sohmiya M, Nishiki M. Regulation of human growth hormone secretion and its disorders. Intern Med. 2002;41(1):7–13. doi:10.2169/internalmedicine.41.7
  • Li Z, Yang Q, Yang Y, Wang D, Wang S. Successful treatment of pachydermoperiostosis with etoricoxib in a patient with a homozygous splice‐site mutation in the SLCO2A1 gene. Br J Dermatol. 2018;180(3):682–684. doi:10.1111/bjd.14480
  • Alessandrella A, Della Casa R, Alessio M, Puente Prieto J, Strisciuglio P, Melis D. A novel homozygous mutation in the SLCO2A1 gene causing pachydermoperiostosis: efficacy of hydroxychloroquine treatment. Am J Med Genet A. 2018;176(5):1253–1257. doi:10.1002/ajmg.a.38677
  • Li X, Hao D, Li-Ling J, Jiang X. Complete form of pachydermoperiostosis with cutis verticis gyrata resulting from the SLCO2A1 gene mutation. Indian J Dermatol Venereol Leprol. 2019;85(6):681. doi:10.4103/ijdvl.IJDVL_911_17
  • Molitch ME. Management of incidentally found nonfunctional pituitary tumors. Neurosurg Clin N Am. 2012;23(4):543–553. doi:10.1016/j.nec.2012.06.003