Pheochromocytoma. A case report

被引：0

作者：

Ripodas, B. ^{[1
]}

Arillo, A. ^{[1
]}

Murie, M. ^{[2
]}

Garcia Garcia, D. ^{[3
]}

机构：

[1] Ctr Salud Chantrea, Pamplona 31015, Spain

[2] Complejo Hosp Navarra, Med Interna Serv, Navarra, Spain

[3] Complejo Hosp Navarra, Serv Urol, Navarra, Spain

来源：

ANALES DEL SISTEMA SANITARIO DE NAVARRA | 2012年 / 35卷 / 01期

关键词：

Pheochromocytoma; Adrenalectomy; Catecholamines; Paraganglioma; Malignity; MALIGNANT ADRENAL-TUMORS; LAPAROSCOPIC ADRENALECTOMY; DIAGNOSIS; BENIGN;

D O I：

10.4321/S1137-66272012000100011

中图分类号：

R1 [预防医学、卫生学];

学科分类号：

1004 ; 120402 ;

摘要：

We present the case of a 34 year-old male, who was diagnosed with a malign pheochromocytoma and who was treated with left laparascopic suprarenalectomy. This is a neoplasia of the chromoffin cells with a prevalence of two cases per million inhabitants, which generally causes the typical symptoms of episodic freeing of catecholamines. We describe the case's form of presentation, which began with successive episodes of intense abdominal pain on the left side. In the abdominal pelvic ultrasound and abdominal CT, a mass of 6.5 cm diameter was objectified, dependent on the left suprarenal gland. High levels of metanefrines and catecholamines were evident in the urine. A total left laparoscopic adrenalectomy was carried out. The pathological anatomy showed malign pheochromocytoma.

引用

收藏

页码：121 / 125

页数：5

相关论文

共 19 条

[1] Pheochromocytoma: State-of-the-art and future prospects [J].

Bravo, EL ;

Tagle, R .

ENDOCRINE REVIEWS, 2003, 24 (04) :539-553

[2] EVOLVING CONCEPTS IN THE PATHOPHYSIOLOGY, DIAGNOSIS, AND TREATMENT OF PHEOCHROMOCYTOMA [J].

BRAVO, EL .

ENDOCRINE REVIEWS, 1994, 15 (03) :356-368

[3]

Edwin B, 2001, BMC Surg, V1, P2

[4] Benign paragangliomas: Clinical presentation and treatment outcomes in 236 patients [J].

Erickson, D ;

Kudva, YC ;

Ebersold, MJ ;

Thompson, GB ;

Grant, CS ;

Van Heerden, JA ;

Young, WF .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (11) :5210-5216

[5] Malignant pheochromocytoma: a review [J].

Harari, Avital ;

Inabnet, William B., III .

AMERICAN JOURNAL OF SURGERY, 2011, 201 (05) :693-701

[6] Use of the Tyrosine Kinase Inhibitor Sunitinib in a Patient with von Hippel-Lindau Disease: Targeting Angiogenic Factors in Pheochromocytoma and Other von Hippel-Lindau Disease-Related Tumors [J].

Jimenez, Camilo ;

Cabanillas, Maria E. ;

Santarpia, Libero ;

Jonasch, Eric ;

Kyle, Karen L. ;

Lano, Elizabeth A. ;

Matin, Surena F. ;

Nunez, Rodolfo F. ;

Perrier, Nancy D. ;

Phan, Alexandria ;

Rich, Thereasa A. ;

Shah, Beejal ;

Williams, Michelle D. ;

Waguespack, Steven G. .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (02) :386-391

[7] Results of laparoscopic adrenalectomy for suspected and unsuspected malignant adrenal neoplasms [J].

Kebebew, E ;

Siperstein, AE ;

Clark, OH ;

Duh, QY .

ARCHIVES OF SURGERY, 2002, 137 (08) :948-951

[8] Biochemical diagnosis of pheochromocytoma - Which test is best? [J].

Lenders, JWM ;

Pacak, K ;

Walther, MM ;

Linehan, WM ;

Mannelli, M ;

Friberg, P ;

Keiser, HR ;

Goldstein, DS ;

Eisenhofer, G .

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (11) :1427-1434

[9] Laparoscopic adrenalectomy for potentially malignant adrenal tumors greater than 5 centimeters [J].

Liao, Chun-Hou ;

Chueh, Shih-Chieh ;

Lai, Ming-Kuen ;

Hsiao, Po-Jen ;

Chen, Jun .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (08) :3080-3083

[10] A survey on adrenal incidentaloma in Italy [J].

Mantero, F ;

Terzolo, M ;

Arnaldi, G ;

Osella, G ;

Masini, AM ;

Alì, A ;

Giovagnetti, M ;

Opocher, G ;

Angeli, A .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (02) :637-644