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  1 / 20284 MEDLINE  
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[PMID]:29397600
[Au] Autor:Weng Y; Xue SN; Zhang SL; Cheng H; Yan L
[Ad] Endereço:Department of Endocrinology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China.
[Ti] Título:[A comparison of clinical characteristics between 2 pedigrees of multiple endocrine neoplasia type 2A with different RET mutations].
[So] Source:Zhonghua Nei Ke Za Zhi;57(2):134-137, 2018 Feb 01.
[Is] ISSN:0578-1426
[Cp] País de publicação:China
[La] Idioma:chi
[Ab] Resumo:Multiple endocrine neoplasia type 2A (MEN2A) is a hereditary syndrome. Here, two different RET proto-oncogen mutation were identified from family members of two MEN2A pedigrees by genetic screening. One RET mutations were found at codons 1893 and 1895 in exon 11 (1893-1895delCGA) from pedigree 1, which is a novel mutation, the other occurs at codon 634 (Cys634Arg) in exon 11 from pedigree 2. However, the clinical characteristics were similar in the patients of the two pedigrees. All the patients were in middle-age at onset. Most of them were firstly diagnosed with bilateral adrenal pheochromocytoma with different degrees of thyroid abnormalities (elevated serum calcitonin with or without thyroid mass, or had been diagnosed with medullary thyroid carcinoma). Some family members were with elevated serum parathyroid hormone but with no other evidences for hyperparathyroidism.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/diagnóstico
Neoplasia Endócrina Múltipla Tipo 2a/genética
Mutação
Feocromocitoma/diagnóstico
Proteínas Proto-Oncogênicas c-ret/genética
[Mh] Termos MeSH secundário: Neoplasias das Glândulas Suprarrenais/genética
Carcinoma Neuroendócrino/diagnóstico
Carcinoma Neuroendócrino/genética
Éxons
Seres Humanos
Meia-Idade
Neoplasia Endócrina Múltipla Tipo 2a/patologia
Linhagem
Feocromocitoma/genética
Mutação Puntual
Neoplasias da Glândula Tireoide/diagnóstico
Neoplasias da Glândula Tireoide/genética
[Pt] Tipo de publicação:COMPARATIVE STUDY; JOURNAL ARTICLE
[Nm] Nome de substância:
EC 2.7.10.1 (Proto-Oncogene Proteins c-ret)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180306
[Lr] Data última revisão:
180306
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180206
[St] Status:MEDLINE
[do] DOI:10.3760/cma.j.issn.0578-1426.2018.02.010


  2 / 20284 MEDLINE  
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[PMID]:29348269
[Au] Autor:Hanna FWF; Issa BG; Sim J; Keevil B; Fryer AA
[Ad] Endereço:Staffordshire University, University Hospital of North Midlands, Stoke-on-Trent, UK Fahmy.hanna@uhns.nhs.uk.
[Ti] Título:Management of incidental adrenal tumours.
[So] Source:BMJ;360:j5674, 2018 01 18.
[Is] ISSN:1756-1833
[Cp] País de publicação:England
[La] Idioma:eng
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/terapia
Gerenciamento Clínico
Guias de Prática Clínica como Assunto
[Mh] Termos MeSH secundário: Neoplasias das Glândulas Suprarrenais/sangue
Neoplasias das Glândulas Suprarrenais/diagnóstico por imagem
Catecolaminas/sangue
Glucocorticoides/sangue
Seres Humanos
Mineralocorticoides/sangue
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Catecholamines); 0 (Glucocorticoids); 0 (Mineralocorticoids)
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180306
[Lr] Data última revisão:
180306
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180120
[St] Status:MEDLINE
[do] DOI:10.1136/bmj.j5674


  3 / 20284 MEDLINE  
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[PMID]:29406048
[Au] Autor:Chaaya G; Morales J; Castiglioni A; Subhani N; Asmar A
[Ad] Endereço:University of Central Florida College of Medicine, Orlando, Florida.
[Ti] Título:Paraganglioma of the Urinary Bladder: A Rare Cause of Hypertension and Urinary Tract Infections.
[So] Source:Am J Med Sci;355(2):191-194, 2018 Feb.
[Is] ISSN:1538-2990
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Pheochromocytoma is a neoplasm, which develops from cells of the chromaffin tissues that are derived from the ectodermic neural system and mostly situated within the adrenal medulla. Approximately 15% of pheochromocytoma cases arise from extra-adrenal chromaffin tissue. Pheochromocytoma of the bladder is rare and accounts for less than 0.06% of all bladder neoplasms and less than 1% of all pheochromocytomas. We report a case of a young woman who presented with uncontrolled hypertension, recurrent urinary tract infections and micturition attacks and was found to have a metastatic bladder paraganglioma. In addition, we provide a summary table of the clinical manifestations of paragangliomas based on anatomic locations.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais
Hipertensão
Neoplasias da Bexiga Urinária
Infecções Urinárias
[Mh] Termos MeSH secundário: Neoplasias das Glândulas Suprarrenais/microbiologia
Neoplasias das Glândulas Suprarrenais/patologia
Neoplasias das Glândulas Suprarrenais/fisiopatologia
Adulto
Feminino
Seres Humanos
Hipertensão/microbiologia
Hipertensão/patologia
Hipertensão/fisiopatologia
Metástase Neoplásica
Feocromocitoma/microbiologia
Feocromocitoma/patologia
Feocromocitoma/fisiopatologia
Feocromocitoma/secundário
Neoplasias da Bexiga Urinária/microbiologia
Neoplasias da Bexiga Urinária/patologia
Neoplasias da Bexiga Urinária/fisiopatologia
Infecções Urinárias/microbiologia
Infecções Urinárias/patologia
Infecções Urinárias/fisiopatologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180301
[Lr] Data última revisão:
180301
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180207
[St] Status:MEDLINE


  4 / 20284 MEDLINE  
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[PMID]:28471119
[Au] Autor:Dai J; Chen SJ; Yang BS; Lü SM; Zhu M; Xu YF; Chen J; Cai HW; Mao W
[Ad] Endereço:Department of Cardiology, Zhejiang Provincial Hospital of Traditional Chinese Medicine, Hangzhou 310006, China.
[Ti] Título:Recurrence of non-cardiogenic pulmonary edema and sustained hypotension shock in cystic pheochromocytoma.
[So] Source:J Zhejiang Univ Sci B;18(5):449-452, 2017 May.
[Is] ISSN:1862-1783
[Cp] País de publicação:China
[La] Idioma:eng
[Ab] Resumo:Pheochromocytoma is a rare neuroendocrine tumor which derives from chromaffin cells of the adrenal gland or relevant to sympathetic nerves and ganglia. The clinical features of pheochromocytoma are various. Paroxysmal episodes of serious hypertension, headache, palpitation, and diaphoresis are the typical manifestations (Bravo, 2004). Hypotension shock, pulmonary edema, and acute coronary syndrome induced by pheochromocytoma are uncommon (Malindretos et al., 2008; Batisse-Lignier et al., 2015). In this study, we present a rare case of cystic pheochromocytoma causing recurrent hypotension shock, non-cardiogenic pulmonary edema, and acute coronary syndrome, and the possible mechanisms are discussed.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/complicações
Neoplasias das Glândulas Suprarrenais/diagnóstico
Feocromocitoma/complicações
Feocromocitoma/diagnóstico
Edema Pulmonar/diagnóstico
Edema Pulmonar/etiologia
Choque/etiologia
[Mh] Termos MeSH secundário: Neoplasias das Glândulas Suprarrenais/terapia
Cistos/complicações
Cistos/diagnóstico
Cistos/terapia
Diagnóstico Diferencial
Feminino
Seres Humanos
Hipotensão/diagnóstico
Hipotensão/etiologia
Hipotensão/terapia
Meia-Idade
Feocromocitoma/terapia
Edema Pulmonar/terapia
Recuperação de Função Fisiológica
Recidiva
Choque/diagnóstico
Choque/prevenção & controle
Resultado do Tratamento
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180226
[Lr] Data última revisão:
180226
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170505
[St] Status:MEDLINE
[do] DOI:10.1631/jzus.B1600411


  5 / 20284 MEDLINE  
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[PMID]:29374711
[Au] Autor:Jung J; Seo J; Kim J; Kim JH
[Ad] Endereço:Department of Life and Nanopharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
[Ti] Título:Ursolic Acid Causes Cell Death in PC-12 Cells by Inducing Apoptosis and Impairing Autophagy.
[So] Source:Anticancer Res;38(2):847-853, 2018 02.
[Is] ISSN:1791-7530
[Cp] País de publicação:Greece
[La] Idioma:eng
[Ab] Resumo:Ursolic acid (UA) is a natural pentacyclic triterpene that has various biological activities, including anticancer and anti-inflammatory effects. This study investigated the ability of UA to cause cell death in pheochromocytoma (PC-12) cells. UA was cytotoxic to PC-12 cells (half-maximum inhibitory concentration=53.2 µM) and significantly reduced the clonogenic ability of PC-12 cells. It also triggered apoptosis by reducing the level of B-cell lymphoma 2 (BCL2), activating caspase-3, and inducing cleavage of poly (ADP-ribosyl) polymerase. To investigate the effects of UA treatment on the induction and progression of autophagy, the levels of p62 and the conversion of the microtubule-associated protein light chain 3 (LC3)-I to LC3-II, which are important markers of autophagic flux, were monitored. UA treatment induced the accumulation of p62 and increased the LC3-II/LC3-I ratio. These results demonstrate that UA treatment induced autophagy, but the downstream signaling pathway was blocked. In summary, this study shows that UA kills PC-12 cells by inducing apoptosis and impairing autophagy progression.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/tratamento farmacológico
Neoplasias das Glândulas Suprarrenais/patologia
Apoptose/efeitos dos fármacos
Autofagia/efeitos dos fármacos
Feocromocitoma/tratamento farmacológico
Feocromocitoma/patologia
Triterpenos/farmacologia
[Mh] Termos MeSH secundário: Animais
Antineoplásicos Fitogênicos/farmacologia
Apoptose/fisiologia
Autofagia/fisiologia
Proliferação Celular/efeitos dos fármacos
Células PC12
Ratos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antineoplastic Agents, Phytogenic); 0 (Triterpenes); P3M2575F3F (ursolic acid)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180221
[Lr] Data última revisão:
180221
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180129
[St] Status:MEDLINE


  6 / 20284 MEDLINE  
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[PMID]:29390427
[Au] Autor:Xu B; Hong Y; Jin M; Li M; Wang C; Wang X
[Ad] Endereço:Department of Urology.
[Ti] Título:Primary adrenal malignant melanoma: A case report and review of literature.
[So] Source:Medicine (Baltimore);96(51):e8956, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: The primary adrenal melanoma (PAM) was an extremely rare occurrence, which was demonstrated as the few cases described in the medical literature. PATIENT CONCERNS: We reported a 58-year-old man who was admitted to hospital because of intermittent left flank pain which lasted for a month. The renal computed tomography (CT) scan showed that a large retroperitoneal tumor measuring 15.5 cm × 12.1 cm × 13.0 cm seemed to have its origin in the left adrenal gland. DIAGNOSES: According to clinical symptoms, previous history, physical examination, and postoperative pathology, the patient was diagnosed as PAM. INTERVENTIONS: The patient was treated with an open procedure for resection of retroperitoneal tumor. After the surgery, the patient participated in the clinical drug trial and received treatment with ipilimumab as adjuvant medical therapy. OUTCOMES: When this article was completed, the patient was still alive and the survival has been already up to 20 months. LESSONS: The PAM was extremely rare in clinic, and its diagnosis and differential diagnosis were difficult. Therefore, clinical physicians should attach great importance to this disease.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/diagnóstico
Neoplasias Pulmonares/diagnóstico
Melanoma/diagnóstico
[Mh] Termos MeSH secundário: Neoplasias das Glândulas Suprarrenais/diagnóstico por imagem
Neoplasias das Glândulas Suprarrenais/patologia
Neoplasias das Glândulas Suprarrenais/terapia
Terapia Combinada
Diagnóstico Diferencial
Seres Humanos
Neoplasias Pulmonares/diagnóstico por imagem
Neoplasias Pulmonares/secundário
Neoplasias Pulmonares/terapia
Masculino
Melanoma/diagnóstico por imagem
Melanoma/secundário
Melanoma/terapia
Meia-Idade
Metástase Neoplásica
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180213
[Lr] Data última revisão:
180213
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180203
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000008956


  7 / 20284 MEDLINE  
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[PMID]:29390591
[Au] Autor:Kan HC; Pang ST; Wu CT; Chang YH; Liu CY; Chuang CK; Lin PH
[Ad] Endereço:Department of Surgery, Division of Urology, Chang Gung Memorial Hospital at Linkou, Taoyuan.
[Ti] Título:Robot-assisted laparoendoscopic single site adrenalectomy: A comparison of 3 different port platforms with 3 case reports.
[So] Source:Medicine (Baltimore);96(51):e9479, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Laparoscopic adrenalectomy is currently the standard of care for adrenal lesion. Minimal invasive laparoscopic surgery such as laparoendoscopic single site surgery (LESS) and natural orifice transluminal endoscopic surgery (NOTES) have been developed to improve cosmetic outcomes and reduce postoperative pain. However, there are still some problems related to instruments and port limitation during LESS surgery. Robot-assisted laparoscopic surgery may help to overcome these problems, and port platforms selection is an important issue. PATIENT CONCERNS: Three cases received robot-assisted LESS adrenalectomy due to adrenal tumor were enrolled. Blood loss, hospital stay, and analgesia injection were compared. DIAGNOSES: Preoperative evaluations were done in a usual manner. Benign tumors were suspect for two patients, while metastatic tumor could not be excluded for the other patient with prior malignancy history. The pathology reports were all benign adrenal cortical adenoma after operation. INTERVENTIONS: Three different port platforms, Da Vinci Single-Site Surgical Platform, GelPOINT, and homemade glove port were used. Trans-peritoneal approach was used for two patients, while the other one received trans-retroperitoneal approach. The advantage and disadvantage of different port platforms were discussed. OUTCOMES: All patients underwent the operation smoothly without major complications or conversion to open surgery. Blood loss amount was small, hospital stay was short, and only one patient received one single dose of opioid analgesia injection after the surgery. LESSONS: The main problems of LESS are the loss of a working triangle and the limitations of the instruments. Robot-assisted LESS may help surgeons overcome part of these problems. Many different port platforms are available, and based on our initial experience, we believe that the GelPoint may be a more suitable platform, for it maintains the endo-wrist function of the Da Vinci instruments, and allows the surgeon to design the position of ports freely to minimize external and internal collision.
[Mh] Termos MeSH primário: Adrenalectomia/métodos
Procedimentos Cirúrgicos Robóticos/métodos
[Mh] Termos MeSH secundário: Adenoma/cirurgia
Neoplasias das Glândulas Suprarrenais/cirurgia
Adrenalectomia/instrumentação
Adulto
Idoso
Feminino
Seres Humanos
Masculino
Meia-Idade
Procedimentos Cirúrgicos Robóticos/instrumentação
[Pt] Tipo de publicação:CASE REPORTS; COMPARATIVE STUDY; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180212
[Lr] Data última revisão:
180212
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180203
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009479


  8 / 20284 MEDLINE  
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[PMID]:29384929
[Au] Autor:Park SY; Kwak MK; Kim HJ; Park HK; Suh KI; Yoo MH; Jin SY; Yun S; Byun DW
[Ad] Endereço:Division of Endocrinology and Metabolism, Departments of Internal Medicine.
[Ti] Título:Case report of a bilateral adrenal myelolipoma associated with Cushing disease.
[So] Source:Medicine (Baltimore);96(52):e9455, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Adrenal myelolipomas are rare benign tumors, composed of a variable mixture of mature adipose tissue and hematopoietic tissue. These tumors are frequently detected incidentally and are usually asymptomatic, and hormonally inactive. PATIENT CONCERNS: During a routine health checkup, a 52-year-old man was found to have a tumor on the bilateral adrenal glands. Abdominal computed tomography revealed a well-defined, heterogeneously enhanced bilateral adrenal mass, suggesting a myelolipoma. DIAGNOSES: The hormonal evaluation revealed adrenocorticotropic hormone (ACTH) dependent Cushing syndrome. INTERVENTIONS: The patient underwent left adrenalectomy, and transsphenoidal resection of a pituitary mass. The final diagnosis was adrenal myelolipoma associated with Cushing disease. OUTCOMES: Growth of right adrenal myelolipoma was detected during the 7-year follow-up. There were enhancing pituitary lesions in repeat magnetic resonance imaging of the sellar region, which implies persistent or recurrent pituitary adenoma. This case reinforces relationship between Cushing disease and adrenal myelolipoma. LESSONS: To the best of our knowledge, this is the first reported pathologically confirmed bilateral adrenal myelolipoma associated with Cushing disease. This report supports the idea that ACTH is associated with the development of adrenal myelolipoma.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/complicações
Neoplasias das Glândulas Suprarrenais/diagnóstico
Mielolipoma/complicações
Mielolipoma/diagnóstico
Hipersecreção Hipofisária de ACTH/complicações
Hipersecreção Hipofisária de ACTH/diagnóstico
[Mh] Termos MeSH secundário: Neoplasias das Glândulas Suprarrenais/cirurgia
Adrenalectomia
Seres Humanos
Masculino
Meia-Idade
Mielolipoma/cirurgia
Hipersecreção Hipofisária de ACTH/cirurgia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180209
[Lr] Data última revisão:
180209
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180201
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009455


  9 / 20284 MEDLINE  
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[PMID]:29193927
[Au] Autor:Alvarado M; Ramirez-Vick M; Allende-Vigo M; Mendez-Latalladi W; Agosto M; Gonzalez R; Martinez M; Vega M; Fernandez M; Velez R; Méndez K
[Ti] Título:Pheochromocytoma in pregnancy: A case Report.
[So] Source:Bol Asoc Med P R;108(1):93-6, 2016.
[Is] ISSN:0004-4849
[Cp] País de publicação:Puerto Rico
[La] Idioma:eng
[Ab] Resumo:This is the case of a 38 year-old female patient with an intrauterine pregnancy, in which a previous incidentally identified adrenal mass proved to be a pheochromocytoma during the antenatal period. The patient was started on α-and ß-adrenergic blockade to maintain hemodynamic stability, and surgical removal of the lesion was performed during the second trimester without major complications. In view of the rarity of this disorder in pregnancy, it is imperative to have a high index of suspicion for a prompt and dedicated management, since this tumor, if unrecognized, is associated with high fetal and maternal mortality.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/diagnóstico
Feocromocitoma/diagnóstico
Complicações Neoplásicas na Gravidez/diagnóstico
[Mh] Termos MeSH secundário: Neoplasias das Glândulas Suprarrenais/cirurgia
Antagonistas Adrenérgicos alfa/uso terapêutico
Antagonistas Adrenérgicos beta/uso terapêutico
Adulto
Feminino
Seres Humanos
Feocromocitoma/cirurgia
Gravidez
Complicações Neoplásicas na Gravidez/cirurgia
Segundo Trimestre da Gravidez
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Adrenergic alpha-Antagonists); 0 (Adrenergic beta-Antagonists)
[Em] Mês de entrada:1712
[Cu] Atualização por classe:171214
[Lr] Data última revisão:
171214
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171202
[St] Status:MEDLINE


  10 / 20284 MEDLINE  
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[PMID]:28740068
[Au] Autor:Junejo SZ; Tuli S; Heimann DM; Sachmechi I; Reich D
[Ad] Endereço:Department of Medicine, Queens Hospital Center, Icahn School of Medicine at Mount Sinai, Jamaica, NY, USA.
[Ti] Título:A Case Report of Cystic Pheochromocytoma.
[So] Source:Am J Case Rep;18:826-829, 2017 Jul 25.
[Is] ISSN:1941-5923
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND Pheochromocytoma is a rare catecholamine-producing tumor with an estimated incidence of less than 0.1% in the global population. We present a case of cystic pheochromocytoma that was diagnosed as an incidental finding. The patient presented with abdominal pain and had a history of hypertension. CASE REPORT A 64-year-old man with hypertension presented with a clinical history of intermittent abdominal pain for one year. He denied sweating, palpitations, headache or back pain. He was found to have an elevated blood pressure of 170/90 and no palpable abdominal mass. Contrast-enhanced computed tomography (CT) imaging of the abdomen and pelvis were performed that showed cystic mass measuring 9 cm in diameter arising from the left adrenal gland with contrast-enhancing mural nodules. Magnetic resonance imaging (MRI) confirmed the cystic nature of the mass. Laboratory analysis showed an elevated plasma normetanephrine (NMN) of 1,087 pg/ml and metanephrine (MN) of 372 pg/ml; 24-hour urine showed elevated levels of NMN and MN, 3,002 mg/24 h and 1,596 mg/24 h, respectively. Given the laboratory and radiologic findings, a diagnosis of cystic pheochromocytoma was made. After controlling blood pressure with the alpha-blocker, doxazosin, the patient was hydrated and scheduled for an elective adrenalectomy. The histopathology of the excised adrenal gland was consistent with a cystic pheochromocytoma. CONCLUSIONS Cystic pheochromocytoma is a very rare tumor that may present without symptoms. The clinical course of cystic pheochromocytoma is similar to that of solid pheochromocytoma. Early surgical intervention is recommended, following blood pressure control with an alpha-blocker, and adequate hydration.
[Mh] Termos MeSH primário: Neoplasias das Glândulas Suprarrenais/diagnóstico
Feocromocitoma/diagnóstico
[Mh] Termos MeSH secundário: Dor Abdominal/etiologia
Seres Humanos
Hipertensão/etiologia
Masculino
Metanefrina/análise
Meia-Idade
Normetanefrina/análise
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0J45DE6B88 (Normetanephrine); 5001-33-2 (Metanephrine)
[Em] Mês de entrada:1712
[Cu] Atualização por classe:171201
[Lr] Data última revisão:
171201
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170726
[St] Status:MEDLINE



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