Well-Differentiated Neuroendocrine Tumor—A Low b-Grade Tumor’s Aggressive Course and Dismal Outcome: A Case Report

Well-Differentiated Neuroendocrine Tumor—A Low b-Grade Tumor’s Aggressive Course and Dismal Outcome: A Case Report

 

Dinesh Atwal, MD; Krishna Prasad Joshi, MD; Susanne Jeffus, MD;
James Ntambi, MD; Fade Mahmoud, MD, FACP

Perm J 2017;21:16-193 [Full Citation]

https://doi.org/10.7812/TPP/16-193
E-pub: 06/14/2017

ABSTRACT

Introduction: Incidence of well-differentiated neuroendocrine tumors (NETs) of the colon and rectum is increasing and is now approximately 1 per 100,000 in the US. NETs are either well-differentiated (indolent) or poorly differentiated (aggressive). The majority of these tumors are found incidentally during screening colonoscopies and rarely are associated with symptoms of hormonal syndrome, even during the advanced stage. Metastatic well-differentiated NETs of the colon and rectum are incurable, hard to treat, and associated with a poor prognosis and survival rates similar to colorectal adenocarcinoma survival.
Case Presentation: A 56-year-old man presented to our clinic with right-sided weakness and a 40-pound weight loss during the previous 2 months. A neurologic examination was remarkable for atrophy of the right trapezius muscle and decreased strength in the right upper extremity. Imaging revealed extensive blastic and lytic lesions involving the axial skeleton, a large rectal mass, a large necrotic nodal mass extending from the left iliac region to the level of the left renal veins, and multiple necrotic liver metastasis. Liver lesion fine-needle aspiration findings were consistent with metastatic well-differentiated neuroendocrine carcinoma.
Discussion: This case illustrates how a low-grade tumor can have an aggressive course with poor outcomes. Metastatic well-differentiated NETs of the colon and rectum remain difficult to treat because evidence is scarce. More research is needed on this topic. 

Introduction

Well-differentiated neuroendocrine tumors (NETs) of the colon and rectum, also known as hindgut carcinoids, are increasingly diagnosed in the US, with an annual incidence of 1 per 100,000.1,2 Most of these tumors are found incidentally during screening colonoscopies. Approximately 50% of patients are asymptomatic, but rectal bleeding, pain, and change in bowel habits may occur for some.3 These tumors rarely cause symptoms of hormonal syndromes such as flushing or diarrhea, even during the metastatic stage.3 The mean age at diagnosis is 56 years.2 In general, NETs are divided into well-differentiated (indolent) and poorly differentiated (aggressive) categories. Well-differentiated (low- and intermediate-grade) NETs also are known as carcinoid tumors or grades 1 and 2 neuroendocrine tumors, respectively.2 Prognosis for early-stage, well-differentiated NETs of the colon and rectum is good, with 5-year overall survival of 88%. Once metastasized, however, these tumors are associated with a poor prognosis similar to prognosis for metastatic colorectal adenocarcinoma, with a 5-year survival rate of 32%.2

Case Presentation

A 56-year-old man with an unremarkable medical history arrived at the Emergency Department with right-sided weakness and an inability to hold objects in his right hand. He also had lost 40 pounds during the previous 2 months. On examination, his cranial nerves were intact and a motor examination was remarkable for atrophy of the right trapezius muscle. Strength was 4/5 in the right upper extremity with decreased muscle tone. Reflexes were 2/4 throughout, and the bilateral Hoffmann sign and bilateral pectoral reflex were absent. A sensory examination was remarkable for decreased pinprick in the right C6-C8 territory. Normal gait and the Romberg sign were not present. The rest of his neurologic examination was unremarkable. Brain magnetic resonance imaging findings were negative for intracranial pathology but revealed lesions in the cervical spine. A cervical spine magnetic resonance image revealed both blastic and lytic lesions involving the skeletal structures but not the spinal cord (Figure 1A and B). A computed tomography (CT) scan of the chest, abdomen, and pelvis with contrast revealed mixed blastic and lytic lesions involving the axial skeleton, a large rectal mass, a large (9-cm) necrotic nodal mass extending from the left iliac regions to the level of the left renal veins, and multiple liver metastasis including a large necrotic mass involving the entire right lobe of the liver that measured 17 x 12 x 13.9 cm. An octreoscan showed increased radiotracer uptake, indicating a rich somatostatin receptor tumor (Figure 2 A-C). Prostate-specific antigen, carcinoembryonic antigen, and alpha-fetoprotein tumor marker findings were negative. Fine-needle aspiration (FNA) of a liver lesion was consistent with metastatic well-differentiated neuroendocrine carcinoma (Cam 5.2 marker, positive [strong and diffuse]; synaptophysin marker, positive [strong and diffuse]; CD56 marker, positive [strong and diffuse]; Figure 3A-C). We obtained another FNA of the large necrotic nodal mass in the left flank, and final pathology was consistent with well-differentiated neuroendocrine carcinoma most likely originating from the rectum. The patient was started on octreotide injections as an outpatient, but he continued to experience disease progression and developed difficulty with urinating and defecating. A repeat CT of the chest, abdomen, and pelvis confirmed disease progression. The patient ultimately required a laparoscopic diverting loop sigmoid colostomy to help him defecate. He subsequently was admitted to hospice care and died. The case timeline appears in Figure 4.

Well-Differentiated Neuroendocrine Tumor—A Low b-Grade Tumor’s Aggressive Course and Dismal Outcome: A Case Report

Well-Differentiated Neuroendocrine Tumor—A Low b-Grade Tumor’s Aggressive Course and Dismal Outcome: A Case Report

Well-Differentiated Neuroendocrine Tumor—A Low b-Grade Tumor’s Aggressive Course and Dismal Outcome: A Case Report

Well-Differentiated Neuroendocrine Tumor—A Low b-Grade Tumor’s Aggressive Course and Dismal Outcome: A Case Report

Discussion

Lack of relevant data makes it a challenge to treat metastatic well-differentiated colorectal NETs.4 Current treatment options are extrapolated from the treatment regimen for midgut NETs; these options include somatostatin analogs, interferon alpha, hepatic arterial embolization, and surgical cytoreduction.4 Chemotherapy is not effective for this disease, and no data support its use for rectal NETs. These colorectal NETs are not associated with carcinoid syndrome; nevertheless, octreotide injections are used for its growth inhibitory effect.5,6 Octreotide injections should be strongly considered, especially if there is evidence of somatostatin receptor expression by increased radiotracer uptake on octreoscan.4 Interferon alpha may be considered when metastatic colorectal NETs progress during octreotide injection treatment; however, the side effect profile is a major issue. Cytoreductive therapy, particularly with liver-only metastasis, can improve quality of life for patients with NETs.4

Disclosure Statement

The author(s) have no conflicts of interest to disclose.

Acknowledgements

Brenda Moss Feinberg, ELS, provided editorial assistance.

How to Cite this Article

Atwal D, Joshi KP, Jeffus S, Ntambi J, Mahmoud F. Well-differentiated neuroendocrine tumor—a low b-grade tumor’s aggressive course and dismal outcome: A case report. Perm J 2017;21:16-193. DOI: https://doi.org/10.7812/TPP/16-193.

References
1.    Yao JC, Phan AT, Chang DZ, et al. Efficacy of RAD001 (everolimus) and octreotide LAR in advanced low- to intermediate-grade neuroendocrine tumors: Results of a phase II study. J Clin Oncol 2008 Sep10;26(26):4311-8. DOI: https://doi.org/10.1200/jco.2008.16.7858. Erratum in: J Clin Oncol 2008 Dec 1;26(34):5660. DOI: https://doi.org/10.1200/JCO.2008.20.5583.
    2.    Modlin IM, Lye KD, Kidd M. A 5-decade analysis of 13,715 carcinoid tumors. Cancer 2003 Feb 15;97(4):934-59. DOI: https://doi.org/10.1002/cncr.11105.
    3.    Wang AY, Ahmad NA. Rectal carcinoids. Curr Opin Gastroenterol 2006 Sep;22(5):529-35. DOI: https://doi.org/10.1097/01.mog.0000239868.27328.1d.
    4.    Ramage JK, Goretzki PE, Manfredi R, et al; Frascati Consensus Conference participants. Consensus guidelines for the management of patients with digestive neuroendocrine tumours: Well-differentiated colon and rectum tumour/carcinoma. Neuroendocrinology 2008;87(1):31-9. DOI: https://doi.org/10.1159/000111036
    5.    Arnold R, Trautmann ME, Creutzfeldt W, et al. Somatostatin analogue octreotide and inhibition of tumour growth in metastatic endocrine gastroenteropancreatic tumours. Gut 1996 Mar;38(3):430-8. DOI: https://doi.org/10.1136/gut.38.3.430.
    6.    Rinke A, Müller HH, Schade-Brittinger C, et al; PROMID Study Group. Placebo-controlled, double-blind, prospective, randomized study on the effect of octreotide LAR in the control of tumor growth in patients with metastatic neuroendocrine midgut tumors: A report from the PROMID Study Group. J Clin Oncol 2009 Oct 1;27(28):4656-63. DOI: https://doi.org/10.1200/jco.2009.22.8510.
 

TPJ20Years

 

The Permanente Journal is celebrating it's 20th anniversary year. We look forward to continuing to bring you more high-quality content during the next 20 years.

Subscriptions

Sponsored by the National Permanente Medical Groups, The Permanente Press publishes The Permanente Journal and books related to Kaiser Permanente and health care.

Circulation

25,000 print readers per quarter, 7,628 eTOC readers, and in 2016, 1.4 million page views on TPJ articles in PubMed from a broad international readership.

Letters

Articles, editorials, letters to the editor, and other material represent the opinion of the authors. Send your comments to permanente.journal@kp.org.


Copyright 2017 The Permanente Journal - Kaiser Permanente. All Rights Reserved.