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European Society of Endocrinology Clinical Practice Guideline for long-term follow-up of patients operated on for a phaeochromocytoma or a paraganglioma.
Plouin PF, Amar L, Dekkers OM, Fassnacht M, Gimenez-Roqueplo AP, Lenders JW, Lussey-Lepoutre C, Steichen O; Guideline Working Group. Plouin PF, et al. Eur J Endocrinol. 2016 May;174(5):G1-G10. doi: 10.1530/EJE-16-0033. Eur J Endocrinol. 2016. PMID: 27048283 Review.
To inform patients and care providers in this context of low-quality evidence, the Guideline Working Group therefore prepared recommendations on the basis of expert consensus. ...High-risk patients (young patients and those with a genetic disease, a la …
To inform patients and care providers in this context of low-quality evidence, the Guideline Working Group therefore prepared …
Genotype-phenotype correlations in pheochromocytoma and paraganglioma: a systematic review and individual patient meta-analysis.
Crona J, Lamarca A, Ghosal S, Welin S, Skogseid B, Pacak K. Crona J, et al. Endocr Relat Cancer. 2019 May;26(5):539-550. doi: 10.1530/ERC-19-0024. Endocr Relat Cancer. 2019. PMID: 30893643 Free PMC article.
Pheochromocytoma and paraganglioma (PPGL) can be divided into at least four molecular subgroups. ...We conclude that molecular categorization accordingly to SDHB provided independent information on the risk of metastasis. Driver mutations status did not correlate in …
Pheochromocytoma and paraganglioma (PPGL) can be divided into at least four molecular subgroups. ...We conclude that molecular catego …
Incidence of pheochromocytoma and sympathetic paraganglioma in the Netherlands: A nationwide study and systematic review.
Berends AMA, Buitenwerf E, de Krijger RR, Veeger NJGM, van der Horst-Schrivers ANA, Links TP, Kerstens MN. Berends AMA, et al. Eur J Intern Med. 2018 May;51:68-73. doi: 10.1016/j.ejim.2018.01.015. Epub 2018 Feb 1. Eur J Intern Med. 2018. PMID: 29361475 Review.
INTRODUCTION: Recent years have seen major changes in clinical practice which may have affected the incidence rates of pheochromocytoma(PCC)/sympathetic paraganglioma(sPGL). There is, however, a lack of up-to-date information describing trends in these incidence rat …
INTRODUCTION: Recent years have seen major changes in clinical practice which may have affected the incidence rates of pheochromocytoma(PCC) …
Composite phaeochromocytomas-a systematic review of published literature.
Dhanasekar K, Visakan V, Tahir F, Balasubramanian SP. Dhanasekar K, et al. Langenbecks Arch Surg. 2022 Mar;407(2):517-527. doi: 10.1007/s00423-021-02129-5. Epub 2021 Mar 2. Langenbecks Arch Surg. 2022. PMID: 33651160 Free PMC article. Review.
RESULTS: There were 62 studies included, with a total of 94 patients. Of 91 patients where data was available, the median (range) age of patients was 48 (4-86) years. Of 90 patients where information was provided, 57% were female. In at least 28 …
RESULTS: There were 62 studies included, with a total of 94 patients. Of 91 patients where data was available, the median (ran …
Ectopic ACTH- and/or CRH-Producing Pheochromocytomas.
Elliott PF, Berhane T, Ragnarsson O, Falhammar H. Elliott PF, et al. J Clin Endocrinol Metab. 2021 Jan 23;106(2):598-608. doi: 10.1210/clinem/dgaa488. J Clin Endocrinol Metab. 2021. PMID: 32710791
STUDY SELECTION: Original articles, including case reports and case series, reporting individual patient data from patients with ACTH- and/or CRH-secreting pheochromocytomas. ...Despite the challenge in diagnosis, patient outcomes appear favorable....
STUDY SELECTION: Original articles, including case reports and case series, reporting individual patient data from patients wi …
MANAGEMENT OF ENDOCRINE DISEASE: Recurrence or new tumors after complete resection of pheochromocytomas and paragangliomas: a systematic review and meta-analysis.
Amar L, Lussey-Lepoutre C, Lenders JW, Djadi-Prat J, Plouin PF, Steichen O. Amar L, et al. Eur J Endocrinol. 2016 Oct;175(4):R135-45. doi: 10.1530/EJE-16-0189. Epub 2016 Apr 14. Eur J Endocrinol. 2016. PMID: 27080352 Review.
Patient follow-up was neither standardized nor exhaustive in the included studies. A clear description of patient retrieval methods was available for nine studies and the follow-up protocol and patient flow for four studies. ...
Patient follow-up was neither standardized nor exhaustive in the included studies. A clear description of patient retrieval me …
Peritoneal carcinomatosis from ovarian paraganglioma: Report of a rare case and systematic review of the literature.
Bizzarri N, De Cian F, Di Domenico S, Centurioni MG, Mammoliti S, Ghirardi V, Vellone VG. Bizzarri N, et al. J Obstet Gynaecol Res. 2018 Sep;44(9):1682-1692. doi: 10.1111/jog.13713. Epub 2018 Jul 6. J Obstet Gynaecol Res. 2018. PMID: 29978527
Paraganglioma is one of the rarest neoplasms involving the ovary, with only 10 previous reports. ...Ovarian paraganglioma is an extremely rare condition. We report the first case of primary malignant ovarian paraganglioma with an exceptionally aggressive beha …
Paraganglioma is one of the rarest neoplasms involving the ovary, with only 10 previous reports. ...Ovarian paraganglioma is a …
Effect of surgical treatment on myocardial strain in patients with pheochromocytoma and paraganglioma: a mini-review and meta-analysis.
Tadic M, Sala C, Carugo S, Cuspidi C. Tadic M, et al. J Endocrinol Invest. 2021 Nov;44(11):2327-2332. doi: 10.1007/s40618-021-01631-3. Epub 2021 Jul 7. J Endocrinol Invest. 2021. PMID: 34235707
AIM: Information on systolic dysfunction, as assessed by left-ventricular (LV) mechanics, in patients with pheochromocytoma after surgical treatment is scanty. ...Studies were identified using MeSH terms and crossing the following search items: "myocardial strain" " …
AIM: Information on systolic dysfunction, as assessed by left-ventricular (LV) mechanics, in patients with pheochromocytoma af …
Pheochromocytoma of the urinary bladder: a systematic review of the contemporary literature.
Beilan JA, Lawton A, Hajdenberg J, Rosser CJ. Beilan JA, et al. BMC Urol. 2013 Apr 29;13:22. doi: 10.1186/1471-2490-13-22. BMC Urol. 2013. PMID: 23627260 Free PMC article. Review.
BACKGROUND: Pheochromocytoma (paraganglioma) of the urinary bladder is a rare tumor. Herein we sought to review the contemporary literature on pheochromocytomas of the urinary bladder in order to further illustrate the presentation, treatment options and outcomes of pat …
BACKGROUND: Pheochromocytoma (paraganglioma) of the urinary bladder is a rare tumor. Herein we sought to review the contemporary lite …
The scalp hair collar and tuft signs: A retrospective multicenter study of 78 patients with a systematic review of the literature.
Bessis D, Bigorre M, Malissen N, Captier G, Chiaverini C, Abasq C, Barbarot S, Boccara O, Bourrat E, El Fertit H, Eschard C, Hubiche T, Lacour JP, Leboucq N, Mahé E, Mallet S, Marque M, Martin L, Mazereeuw-Hautier J, Milla N, Phan A, Plantin P, Picot MC, Puzenat E, Rigau V, Vabres P, Fraitag S, Boralevi F; Groupe de Recherche Clinique en Dermatologie Pédiatrique. Bessis D, et al. J Am Acad Dermatol. 2017 Mar;76(3):478-487. doi: 10.1016/j.jaad.2016.08.046. Epub 2016 Oct 11. J Am Acad Dermatol. 2017. PMID: 27742172 Review.
METHODS: A 10-year multicenter retrospective and prospective analysis of clinical, radiologic, and histopathologic features of HCS and HTS in pediatric patients was performed. RESULTS: Of the 78 patients included in the study, 56 underwent cranial and brain imaging. …
METHODS: A 10-year multicenter retrospective and prospective analysis of clinical, radiologic, and histopathologic features of HCS and HTS i …
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