Pheochromocytoma With Nonspecific Aortoarteritis: an Unusual Association
نویسندگان
چکیده
Article history: Received: 25 Jan 2011 Revised: 20 Mar 2011 Accepted: 03 Apr 2011
منابع مشابه
Systemic lupus erythematosus with aortoarteritis.
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder, the incidence of which, in prepubertal children is quite rare(l). The diagnostic clinical criteria as suggested by the American Rheumatology Association (ARA) are well known(2). The most specific diagnostic laboratory finding is the presence of antibody to double-standard DNA (ds DNA)(3). We report a child with SLE and idi...
متن کاملPheochromocytoma Presenting with Acute Abdomen.
Pheochromocytoma, a neuroendocrine tumor of the adrenal medulla, arising from chromaffin cells, usually presents with the clinical triad of paroxysmal headache, profuse sweating and palpitations, associated with labile hypertension. Here, we present the case of an adult male with an unusual manifestation of pheochromocytoma in the form of acute pain abdomen with nausea and abdominal guarding, m...
متن کاملMalignant hypertension in children in India.
BACKGROUND Malignant hypertension is now an uncommon entity in the western world but still remains a significant problem in India. Therefore we studied the aetiological spectrum, management, and outcome of these patients. METHODS Forty consecutive children (<16 years) with malignant hypertension were admitted and investigated to exclude or confirm the secondary causes of hypertension. For acu...
متن کاملVasculitis--Indian perspective.
large Vessel Vasculitis Non-specific Aortoarteritis (Takayasu’s arteritis) Aortoarteritis has been well described and studied from India.6Two monograms written by Indian authors are available on the subject.10,11 In contrast to Japanese patients in whom proximal aorta involvement is common ( %), in Indian patients descending and especially abdominal aorta involvement (reversed coarctation) is c...
متن کاملPheochromocytoma Diagnosis After an Abnormal Stress Test: Case Report and Review of the Literature.
Pheochromocytoma is a rare adrenal gland tumor that is often difficult for physicians to diagnose because of its general, nonspecific complaints. Diagnosis is particularly difficult in patients with neurofibromatosis 1, because pheochromocytoma in these patients will mimic other cardiovascular abnormalities. The authors report the case of a 60-year-old woman with an extensive history of hyperli...
متن کامل