Atypical presentations of Phaeochromocytoma – a clinical case report
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://revista.spmi.pt/index.php/rpmi/article/view/1494 |
Resumo: | Introduction: Phaeochromocytoma is a rare neuroendocrine tumour. The biochemical and clinical features derive mainly from excessive catecholamine production. When there is mass necrosis, these tumours may reveal themselves through a huge release of hormones. We present the case of a 42 year old female attending a Hypertension outpatient clinic because of fainting episodes and high blood pressure. She was diagnosed with hypertension at the age of 18 years and was being treated for severe depression.She had no complaints until 3 months earlier when she started suffering from “hard-to-assess” episodes of fatigue, trembling, headache, blurred vision and faintness. SBP was 160-200 mmHg. She had a slow psychomotor response and reduced facial expression. She presented with inconsistently elevated urinary metanephrines and CT scan showed a 3.4 cm mass, with a necrotic center, in her left adrenal gland. Phaeochromocytoma was confirmed with an IMBG scintigraphy. She underwent laparoscopic removal of the mass and histology revealed phaeochromocytoma.Discussion: A diagnosis of Phaeochromocytoma is hard to make because of a number of factors: the rising number of incidentalomas; the technical difficulty in combining biochemical and imaging exams; numerous drug interactions with biochemical results as well as a lack of clinical suspicion when facing unusual presenting features, such as hypotension. Tumour necrosis is usually associated with devastating clinical presentations, which were not present in this patient. |
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Atypical presentations of Phaeochromocytoma – a clinical case reportApresentações atípicas de feocromocitoma, a propósito de um caso clínicofeocromocitomaatípiconão secretornecrosemalignophaeochromocytomaatypicalnecrosismalignancynon-secretingIntroduction: Phaeochromocytoma is a rare neuroendocrine tumour. The biochemical and clinical features derive mainly from excessive catecholamine production. When there is mass necrosis, these tumours may reveal themselves through a huge release of hormones. We present the case of a 42 year old female attending a Hypertension outpatient clinic because of fainting episodes and high blood pressure. She was diagnosed with hypertension at the age of 18 years and was being treated for severe depression.She had no complaints until 3 months earlier when she started suffering from “hard-to-assess” episodes of fatigue, trembling, headache, blurred vision and faintness. SBP was 160-200 mmHg. She had a slow psychomotor response and reduced facial expression. She presented with inconsistently elevated urinary metanephrines and CT scan showed a 3.4 cm mass, with a necrotic center, in her left adrenal gland. Phaeochromocytoma was confirmed with an IMBG scintigraphy. She underwent laparoscopic removal of the mass and histology revealed phaeochromocytoma.Discussion: A diagnosis of Phaeochromocytoma is hard to make because of a number of factors: the rising number of incidentalomas; the technical difficulty in combining biochemical and imaging exams; numerous drug interactions with biochemical results as well as a lack of clinical suspicion when facing unusual presenting features, such as hypotension. Tumour necrosis is usually associated with devastating clinical presentations, which were not present in this patient.Introdução: Os feocromocitomas são tumores neuroendócrinos raros. Tanto as suas características bioquímicas como clínicas resultam maioritariamente da produção excessiva de catecolaminas. Contudo, por vezes existem tumores cuja primeira manifestação se deve a uma libertação maciça de catecolaminas por necrose tumoral. Apresentamos o caso de uma mulher de 42 anos referenciada à consulta por lipotimia e HTA. Antecedentes de HTA desde os 18 anos e Síndroma Depressiva Major sob farmacoterapia.Sem queixas até 3 meses antes, altura em que surgiram episódios dificilmente valorizáveis, caracterizados por astenia, tremor muscular generalizado, cefaleias, visão enevoada e lipotimia. PAS entre 160-200 mmHg. Apresentava lentificação psicomotora e aninamia. O estudo complementar realizado mostrou valores inconstantes de metanefrinas urinárias elevadas e a TC das suprarenais revelou massa supra-renal esquerda de 3,4cm, capsulada com centro necrótico, confirmada por cintigrafia de corpo inteiro com IMBG. Submetida a cirurgia excisional laparascópica electiva que confirmou feocromocitoma.Discussão: O diagnóstico de feocromocitoma revela-se difícil devido ao aumento de incidentalomas, à dificuldade técnica de combinar resultados de métodos bioquímicos e imagiológicos, às interacções medicamentosas com resultados bioquímicos, e ainda à dificuldade de integração de semiologia mais invulgar, como hipotensão. A necrose tumoral nos feocromocitomas está habitualmente associada a quadros devastadores.Sociedade Portuguesa de Medicina Interna2008-12-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://revista.spmi.pt/index.php/rpmi/article/view/1494Internal Medicine; Vol. 15 No. 4 (2008): Outubro/ Dezembro; 268-271Medicina Interna; Vol. 15 N.º 4 (2008): Outubro/ Dezembro; 268-2712183-99800872-671Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://revista.spmi.pt/index.php/rpmi/article/view/1494https://revista.spmi.pt/index.php/rpmi/article/view/1494/1033Ruivo, JorgeTomada, AnaAlcântara, Paulainfo:eu-repo/semantics/openAccess2023-01-07T06:10:43Zoai:oai.revista.spmi.pt:article/1494Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:29:39.894445Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Atypical presentations of Phaeochromocytoma – a clinical case report Apresentações atípicas de feocromocitoma, a propósito de um caso clínico |
title |
Atypical presentations of Phaeochromocytoma – a clinical case report |
spellingShingle |
Atypical presentations of Phaeochromocytoma – a clinical case report Ruivo, Jorge feocromocitoma atípico não secretor necrose maligno phaeochromocytoma atypical necrosis malignancy non-secreting |
title_short |
Atypical presentations of Phaeochromocytoma – a clinical case report |
title_full |
Atypical presentations of Phaeochromocytoma – a clinical case report |
title_fullStr |
Atypical presentations of Phaeochromocytoma – a clinical case report |
title_full_unstemmed |
Atypical presentations of Phaeochromocytoma – a clinical case report |
title_sort |
Atypical presentations of Phaeochromocytoma – a clinical case report |
author |
Ruivo, Jorge |
author_facet |
Ruivo, Jorge Tomada, Ana Alcântara, Paula |
author_role |
author |
author2 |
Tomada, Ana Alcântara, Paula |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Ruivo, Jorge Tomada, Ana Alcântara, Paula |
dc.subject.por.fl_str_mv |
feocromocitoma atípico não secretor necrose maligno phaeochromocytoma atypical necrosis malignancy non-secreting |
topic |
feocromocitoma atípico não secretor necrose maligno phaeochromocytoma atypical necrosis malignancy non-secreting |
description |
Introduction: Phaeochromocytoma is a rare neuroendocrine tumour. The biochemical and clinical features derive mainly from excessive catecholamine production. When there is mass necrosis, these tumours may reveal themselves through a huge release of hormones. We present the case of a 42 year old female attending a Hypertension outpatient clinic because of fainting episodes and high blood pressure. She was diagnosed with hypertension at the age of 18 years and was being treated for severe depression.She had no complaints until 3 months earlier when she started suffering from “hard-to-assess” episodes of fatigue, trembling, headache, blurred vision and faintness. SBP was 160-200 mmHg. She had a slow psychomotor response and reduced facial expression. She presented with inconsistently elevated urinary metanephrines and CT scan showed a 3.4 cm mass, with a necrotic center, in her left adrenal gland. Phaeochromocytoma was confirmed with an IMBG scintigraphy. She underwent laparoscopic removal of the mass and histology revealed phaeochromocytoma.Discussion: A diagnosis of Phaeochromocytoma is hard to make because of a number of factors: the rising number of incidentalomas; the technical difficulty in combining biochemical and imaging exams; numerous drug interactions with biochemical results as well as a lack of clinical suspicion when facing unusual presenting features, such as hypotension. Tumour necrosis is usually associated with devastating clinical presentations, which were not present in this patient. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-12-31 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://revista.spmi.pt/index.php/rpmi/article/view/1494 |
url |
https://revista.spmi.pt/index.php/rpmi/article/view/1494 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://revista.spmi.pt/index.php/rpmi/article/view/1494 https://revista.spmi.pt/index.php/rpmi/article/view/1494/1033 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Medicina Interna |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Medicina Interna |
dc.source.none.fl_str_mv |
Internal Medicine; Vol. 15 No. 4 (2008): Outubro/ Dezembro; 268-271 Medicina Interna; Vol. 15 N.º 4 (2008): Outubro/ Dezembro; 268-271 2183-9980 0872-671X reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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