dostęp otwarty

Tom 6, Nr 2 (2021)
Opis przypadku
Opublikowany online: 2021-01-25
Pobierz cytowanie

Oligosymptomatic neuroendocrine neoplasm of the small intestine with metastases spread to the heart, bones, muscles and intraperitoneally after a few years in remission – diagnostic and therapeutic challenges

Natalia Tyrybon1, Agnieszka Żyłka1, Joanna Długosińska1, Małgorzata Benke1, Marek Dedecjus1
Biuletyn Polskiego Towarzystwa Onkologicznego Nowotwory 2021;6(2):132-135.
Afiliacje
  1. Department of Endocrine Oncology and Nuclear Medicine, M. Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland

dostęp otwarty

Tom 6, Nr 2 (2021)
Opis przypadku / Case report
Opublikowany online: 2021-01-25

Streszczenie

A fifty-one-year-old male patient with a history of recurring abdominal pains and signs of subileus, without carcinoid syndrome signs, underwent a laparatomy with a resection of the small intestine segment. Histopathology revealed a well- -differentiated neuroendocrine neoplasm of the small intestine. Due to the lack of hormonal activity and low malignancy potential the patient was not qualified for adjuvant therapy. The yearly computed tomography did not indicate a recurrence of the neoplasm. The patient did not report any “red flag” symptoms. After a few years in remission [68Ga]-DOTATATE PET/CT revealed a dynamic development of the illness. The patient was qualified for palliative treatment with long-acting somatostatin analogue. Due to the treatment’s ineffectiveness and further progression of the disease, the patient received Peptide Receptor Radionuclide Therapy (PRRT). In spite of the therapy his condition did not improve and progression was observed. The patient died because of a malfunction of the cardiac conduction system caused by metastases in the heart.

Streszczenie

A fifty-one-year-old male patient with a history of recurring abdominal pains and signs of subileus, without carcinoid syndrome signs, underwent a laparatomy with a resection of the small intestine segment. Histopathology revealed a well- -differentiated neuroendocrine neoplasm of the small intestine. Due to the lack of hormonal activity and low malignancy potential the patient was not qualified for adjuvant therapy. The yearly computed tomography did not indicate a recurrence of the neoplasm. The patient did not report any “red flag” symptoms. After a few years in remission [68Ga]-DOTATATE PET/CT revealed a dynamic development of the illness. The patient was qualified for palliative treatment with long-acting somatostatin analogue. Due to the treatment’s ineffectiveness and further progression of the disease, the patient received Peptide Receptor Radionuclide Therapy (PRRT). In spite of the therapy his condition did not improve and progression was observed. The patient died because of a malfunction of the cardiac conduction system caused by metastases in the heart.

Pobierz cytowanie

Słowa kluczowe

neuroendocrine neoplasm; carcinoid syndrome; somatostatin analogue; radioisotope therapy

Informacje o artykule
Tytuł

Oligosymptomatic neuroendocrine neoplasm of the small intestine with metastases spread to the heart, bones, muscles and intraperitoneally after a few years in remission – diagnostic and therapeutic challenges

Czasopismo

Biuletyn Polskiego Towarzystwa Onkologicznego Nowotwory

Numer

Tom 6, Nr 2 (2021)

Typ artykułu

Opis przypadku

Strony

132-135

Opublikowany online

2021-01-25

Wyświetlenia strony

181

Wyświetlenia/pobrania artykułu

94

Rekord bibliograficzny

Biuletyn Polskiego Towarzystwa Onkologicznego Nowotwory 2021;6(2):132-135.

Słowa kluczowe

neuroendocrine neoplasm
carcinoid syndrome
somatostatin analogue
radioisotope therapy

Autorzy

Natalia Tyrybon
Agnieszka Żyłka
Joanna Długosińska
Małgorzata Benke
Marek Dedecjus

Referencje (15)
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