Literature DB >> 8405477

A review of clinicopathologic features of pheochromocytomas in Hong Kong Chinese.

K Y Lam1, A C Chan, W M Wong, K S Lam.   

Abstract

Twenty-two Chinese patients with pheochromocytomas including 18 surgical and four autopsy cases were reported. The incidence at autopsy was 0.048%. The tumours were most common in the sixth and the fourth decades in males and females, respectively. There was no sex predilection. The incidence of bilaterality was 4.5% and the tumours were more common on the right side. 9.1% of the tumours were malignant and they were larger than their benign counterparts. Solid and diffuse pattern and mixed pattern were the most common histologic patterns. Minor histological features included hyaline globules (64%), nuclear pseudo-inclusions (55%), lipid degeneration (4.5%) and peri-adrenal brown fat (18%). All of them were strongly positive for the three pan-neuroendocrine markers (neuron-specific enolase, synaptophysin and chromogranin) confirming the usefulness of these markers in diagnosing pheochromocytoma.

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Year:  1993        PMID: 8405477

Source DB:  PubMed          Journal:  Eur J Surg Oncol        ISSN: 0748-7983            Impact factor:   4.424


  8 in total

Review 1.  Adrenal oncocytic phaeochromocytoma with putative adverse histologic features: a unique case report and review of the literature.

Authors:  Kais Kasem; Alfred K-Y Lam
Journal:  Endocr Pathol       Date:  2014-12       Impact factor: 3.943

2.  The clinicopathological features and importance of p53, Rb, and mdm2 expression in phaeochromocytomas and paragangliomas.

Authors:  K Y Lam; C Y Lo; N M Wat; J M Luk; K S Lam
Journal:  J Clin Pathol       Date:  2001-06       Impact factor: 3.411

Review 3.  Update on Adrenal Tumours in 2017 World Health Organization (WHO) of Endocrine Tumours.

Authors:  Alfred King-Yin Lam
Journal:  Endocr Pathol       Date:  2017-09       Impact factor: 3.943

Review 4.  Hereditary paraganglioma targets diverse paraganglia.

Authors:  B E Baysal
Journal:  J Med Genet       Date:  2002-09       Impact factor: 6.318

5.  Composite Pheochromocytoma-Ganglioneuroma of the Adrenal Gland: An Uncommon Entity with Distinctive Clinicopathologic Features.

Authors:  King-Yin Lam; Chung-Yau Lo
Journal:  Endocr Pathol       Date:  1999       Impact factor: 3.943

6.  Perioperative management of pheochromocytoma and catecholamine-induced dilated cardiomyopathy in a pediatric patient.

Authors:  Yuvraj Kalra; Hemant S Agarwal; Andrew H Smith
Journal:  Pediatr Cardiol       Date:  2012-11-07       Impact factor: 1.655

7.  Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma.

Authors:  Jean-Pierre Bayley; Ivonne van Minderhout; Marjan M Weiss; Jeroen C Jansen; Peter H N Oomen; Fred H Menko; Barbara Pasini; Barbara Ferrando; Nora Wong; Lesley C Alpert; Rosie Williams; Edward Blair; Peter Devilee; Peter E M Taschner
Journal:  BMC Med Genet       Date:  2006-01-11       Impact factor: 2.103

8.  A 10-Year Tertiary Care Center Experience With Adrenalectomies for Adrenal Tumors.

Authors:  Mohammad A Alghafees; Ziyad F Musalli; Khalaf Albaqami; Muhannad Q Alqirnas; Meshari A Alqahtani; Faisal Alrasheed; Ahmed Alasker
Journal:  Cureus       Date:  2022-02-06
  8 in total

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