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Number of results

Journal

2014 | 10 | 1 |

Article title

The local spread of pheochromocytoma after
adrenalectomy with a rupture of the tumor capsule
at the time of the surgery

Content

Title variants

Languages of publication

EN

Abstracts

EN
Introduction: We present a case of a 29-year-old
patient treated due to fully symptomatic pheochromocytoma
of the right adrenal gland. Case presentation: Patient was operated on and an open
right-sided adrenalectomy was performed. At the time of
the surgery, a rupture of the tumor capsule occurred. Five
years post-operatively, a recurrence of the symptoms of
chromaffin-cell tumor was noted. After the exact localization
of the multiple recurrences, the patient was reoperated
on. Conclusion: The case of pheochromocytoma is presented
due to the possibility of chromaffin-cell seeding into the
peritoneum, with no signs of distal metastases so far.

Publisher

Journal

Year

Volume

10

Issue

1

Physical description

Dates

accepted
17 - 6 - 2015
received
3 - 1 - 2015
online
4 - 8 - 2015

Contributors

  • Clinic of General and Thoracic Surgery, Medical
    University of Warsaw, Banacha 1a St. 02-097 Warsaw, Poland
  • Clinic of General and Thoracic Surgery, Medical
    University of Warsaw, Banacha 1a St. 02-097 Warsaw, Poland
author
  • Clinic of General and Thoracic Surgery, Medical
    University of Warsaw, Banacha 1a St. 02-097 Warsaw, Poland
author
  • Clinic of General and Thoracic Surgery, Medical
    University of Warsaw, Banacha 1a St. 02-097 Warsaw, Poland
author
  • Clinic of Internal Medicine, Hypertensiology and Angiology,
    Medical University of Warsaw, Banacha 1a St. 02-097 Warsaw,
    Poland
  • Multidisciplinary Hospital
    Warsaw-Miedzylesie, Warsaw, Poland
  • Clinic of General and Thoracic Surgery, Medical
    University of Warsaw, Banacha 1a St. 02-097 Warsaw, Poland

References

  • [1] Sporny S, Musiał J. Markers of malignancy in pheochromocytoma.Endokrynol Pol 2005; 6:946-951
  • [2] Kajor M, Ziaja J, Lange D et al. Analysis of morphology ofadrenal pheochromocytoma as regards their potentialmalignancy. Endokrinol Pol 2005; 6:911-916
  • [3] Geatti O, Shapiro B, Virgolini L. Late presentation of metastaticpheochromocytoma: a problem case solved by I-131 MIBGscintigraphy. Clin Nucl Med. 1990; 15:101-104[Crossref]
  • [4] Zografos GN, Vasiliadis G, Farfaras AN, et al. Laparoscopicsurgery for malignant adrenal tumors. JSLS 2009; 13:196-202
  • [5] Pogorzelski R, Toutounchi S, Fiszer P, Krajewska E, GórnickaB, Zapała Ł, Szostek M, Jakuczun W, Tworus R, Wołoszko T,Skórski M. Regressive changes in phaeochromocytomas andparoxysmal hypertension. CEJMED 2014; 9: 663-666[WoS]
  • [6] Belowska-Bień K, Kucharski W, Janczak D, et al. Pheochromocytomaof the adrenal gland selectively secreting dopamine– a case report. Endokrynol Pol. 2012; 63: 391-395
  • [7] Rutkowska J, Bandurska-Stankiewicz E, Kuglarz E, et al. Adrenaloncocytoma – a case report. Endokrynol Pol. 2012; 63: 308-311
  • [8] Lubikowski J, Kiedrowicz B, Szajko M, et al. Laparoscopicadrenalectomy for functioning and non-functioning adrenaltumors. Endokrynol Pol. 2011; 62:512-516
  • [9] Podgórska J, Cieszanowski A, Bednarczuk T. Adrenal imaging.Endokrynol Pol. 2012; 63:71-81
  • [10] Fliedner SMJ, Lehnert H, Pacak K. Metastatic paraganglioma.Semin Oncol. 2010; 37:627-637[WoS][Crossref]

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_1515_med-2015-0049
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