Atypical presentations of Phaeochromocytoma – a clinical case report

Detalhes bibliográficos
Autor(a) principal: Ruivo, Jorge
Data de Publicação: 2008
Outros Autores: Tomada, Ana, Alcântara, Paula
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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spelling 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
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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
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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
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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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