PHEOCOROMOCYTOMA; A CASE REPORT

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NOORI N.; MOHAMMADI POUR A.; KARIMI MEHRBOD; TOUHIDI M.R.

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Journal: Iranian Journal of Pediatrics Year:2007 | Volume:17 | Issue:1 (SUPPLEMENT) Page(s): 121-124

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Title

PHEOCOROMOCYTOMA; A CASE REPORT

Author(s)

NOORI N. | MOHAMMADI POUR A. | KARIMI MEHRBOD | TOUHIDI M.R. | Issue Writer Certificate

Keywords

PHEOCHROMOCYTOMAQ3

HYPERTENSIONQ3

ABDOMINAL MASSQ3

CHROMEFFINQ3

CATECHOLAMINEQ3

Abstract

Objective: PHEOCHROMOCYTOMA is a neoplosia of chromaffin cells that is very rare in children. Its signs and symptoms result from the release of CATECHOLAMINE. It is usually a solitary, unilateral encapsulated tumor. The predominant clinical findings are crises of HYPERTENSION, palpitation, abdominal pain, paleness, vomiting, sweating, and weight loss. Its diagnosis requires a certain degree of suspicion.Case report: We report on a 3-year-old child with PHEOCHROMOCYTOMA of difficult clinical management. Diagnosis was confirmed by anatomico-phathological study. The patient recovered after surgical resection of the tumor.Conclusion: The patient was a rare case of PHEOCHROMOCYTOMA, his problems being especially HYPERTENSION and was cured after surgical resection of the tumor. This demonstrates the beneficial effect of early diagnosis and treatment.

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APA: Copy

NOORI, N., MOHAMMADI POUR, A., KARIMI, MEHRBOD, & TOUHIDI, M.R.. (2007). PHEOCOROMOCYTOMA; A CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS, 17(1 (SUPPLEMENT)), 121-124. SID. https://sid.ir/paper/76058/en

Vancouver: Copy

NOORI N., MOHAMMADI POUR A., KARIMI MEHRBOD, TOUHIDI M.R.. PHEOCOROMOCYTOMA; A CASE REPORT. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2007;17(1 (SUPPLEMENT)):121-124. Available from: https://sid.ir/paper/76058/en

IEEE: Copy

N. NOORI, A. MOHAMMADI POUR, MEHRBOD KARIMI, and M.R. TOUHIDI, “PHEOCOROMOCYTOMA; A CASE REPORT,” IRANIAN JOURNAL OF PEDIATRICS, vol. 17, no. 1 (SUPPLEMENT), pp. 121–124, 2007, [Online]. Available: https://sid.ir/paper/76058/en

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