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Korean J Abdom Radiol. 2021;5(1):57-62

Publication date (electronic) : 2021 July 15

doi : https://doi.org/10.52668/kjar.2021.00073

Hye-Won Lee, Hong Il Ha

Department of Radiology, Hallym University Sacred Heart Hospital, Anyang-si, Korea

이혜원, 하홍일

한림대학교성심병원 영상의학과

Correspondence: Hong Il Ha, MD, PhD Department of Radiology, Hallym University Sacred Heart Hospital, 22, Gwanpyeong-ro 170beon-gil, Dongan-gu, Anyang-si, Gyeonggi-do 14068, Korea Tel: +82-31-380-3880 E-mail: ha.hongil@gmail.com

Received 2021 June 15; Revised 2021 June 23; Accepted 2021 June 23.

Abstract

Trans Abstract

Introduction

Granulocyte colony-stimulating factor (G-CSF) is a kind of cytokine that belongs to the hematopoietin family. It regulates the leukocyte growth and maturation in the bone marrow [1]. The common cytotoxic agents decrease the production of progenitor cells of the marrow. If the nadir neutrophil count is under 500/uL, the risk of death is markedly increased. G-CSF is broadly used to augment bone marrow production of polymorphonuclear leukocytes and reverse chemotherapeutic agent-induced neutropenia [2]. However, recently, some cases have reported G-CSF-induced large vessel vasculitis. It is an infrequent adverse effect of G-CSF, and there are few reviews on published articles. We report a case of G-CSF-induced aortitis in a patient who was on adjuvant chemotherapy for breast cancer, and we thoroughly review this disease entity with published articles and our case.

Case Report

A 54-year-old female, who had been diagnosed with breast cancer, visited the emergency department eleven days after her first adjuvant chemotherapy cycle with doxorubicin and cyclophosphamide. She complains of a fever, and an emergent laboratory exam shows severe neutropenia (absolute neutrophil count: 96/uL). A long-acting glycosylated G-CSF (lenograstim) was initiated with intravenous (IV) antibiotics (tazobactam) to revise the neutropenia. After two days, her fever was subsided, the neutrophil count was increased, and C-reactive protein (CRP) was slightly decreased (66.16 mg/dL). After then, she has discharged.

However, she visited the emergency department four days after discharge for abdominal and back pain. On laboratory exam, an elevated CRP level (98.02 mg/dL) was noted. She underwent abdomen-pelvis computed tomography (CT) for evaluation. Previously, she took baseline abdomen-pelvis CT, 43 days before the onset of symptom, and there was no remarkable finding (Fig. 1A). However, A newly developed soft-tissue density lesion encases the abdominal aorta with mild enhancement (Fig. 1B) at this time. The lesion was extended from the diaphragmatic crura to the bilateral renal vein level. It was suspected of aortitis, but the possible malignancy could not be excluded. She underwent ¹⁸F-fluorodeoxyglucose positron emission tomography-computed tomography (¹⁸F -FDG-PET/CT) for further evaluation. It revealed a thickening of the suprarenal abdominal aorta wall with strong FDG uptake (Fig. 2A, 2B) without other abnormality. When considering the medical history and radiologic findings, abdominal aortitis induced by G-CSF was strongly suspected. Serum rheumatoid factor and fluorescent antinuclear antibody tests were negative.

Fig. 1.

(A) Baseline abdomen-pelvis CT reveals normal abdominal aorta without any inflammatory condition. (B) After the onset of the symptom, initial abdomen-pelvis CT reveals newly developed diffuse soft tissue density encasing suprarenal abdominal aorta (arrows). (C) On the second follow-up abdomen-pelvis CT, aortitis is improved without any significant sequelae or complication.

Fig. 2.

Disease manifestation on PET/CT. (A), (B) Initial ¹⁸F-FDG-PET/CT reveals increased metabolism around the abdominal aorta (arrows). (C), (D) Follow-up ¹⁸F-FDG-PET/CT after steroid therapy reveals improvement of aortitis.

The treatment with intravenous steroids was immediately initiated the following day after diagnosis. The CRP levels decreased rapidly, and the patient was discharged a few days later, following a rapid clinical improvement. After the high-dose steroid therapy, the dose tapering followed. A follow-up abdomen-pelvis CT scan was conducted 18 days after the second admission, and a second follow-up abdomen-pelvis CT scan 16 days after the first follow-up CT show improved aortitis with residual granulation tissue (Fig.1C). Follow-up ¹⁸F -FDG-PET/CT shows normalized metabolism in the involved area (Fig. 2C, 2D). The entire disease course is summarized in Figure 3.

Fig. 3.

The schematic visualization of the case patient’s disease course.

The patient restarted the chemotherapy cycle without prophylactic G-CSF, and there was no recurrence of aortitis and no development of any associated complications.

Discussion

There are few reported cases with G-CSF-induced aortitis. When reviewed for previously published articles, except for one male case, most of the patients are women diagnosed with breast cancer who had been initiated chemotherapy with prophylactic G-CSF therapy. Two of the cases are remarkable because they did not have any underlying disease [3, 4]. It suggests that some cases of aortitis seem to be caused by the G-CSF use rather than the chemotherapy agent.

Our case patient was diagnosed based on the symptom, medical history, serum markers, and radiologic findings, including abdominal CT and PET-CT. Similarly, reported cases were diagnosed by imaging modalities such as CT, magnetic resonance imaging (MRI), ultrasonography, and PET-CT. The most frequently used diagnostic tool was CT and PET-CT. CT may demonstrate thickening of the aortic wall and periaortic inflammation, although milder degrees of inflammation or wall edema may not be apparent [5]. CT is used in the long-term follow-up of patients with treated aortitis, particularly for monitoring the progression of aortic aneurysm. MR angiography also can depict an area of active aortitis that appears as vessel wall edema, enhancement, or wall thickening [6]. Recently, the use of ¹⁸F-FDG-PET/CT has emerged as a potential tool for the initial diagnosis and assessment of disease activity of aortitis [7]. Serum markers, including CRP and erythrocyte sedimentation rate, are easy ways to follow up and determine the endpoint of steroid therapy. Most reported patients have initiated G-CSF agents such as filgrastim or pegylated-filgrastim, but our case patient used G-CSF, which is the first reported case for this agent.

In a large vessel vasculitis, there are many reported complications such as aneurysm, stenosis, dissection, and even rupture [8]. Some reported G-CSF-induced vasculitis cases revealed aortic dissection [9], iliac artery aneurysms [4], and left pleural effusion [10]. It is recommended for suspected G-CSF-induced aortitis patients to undergo follow-up contrast-enhanced CT to evaluate the subacute or late complications.

G-CSF-induced aortitis is usually resolved spontaneously. However, a case shows long-term involvement of the G-CSF-induced aortitis [4]. There is a possibility of developing severe complications like in other large vessel vasculitides [8]. Thus, prompt diagnosis and rapid initiation of steroid therapy are essential for G-CSF-induced aortitis. Our case patient was treated based on this regimen [11, 12]: IV methylprednisolone 500 mg/day for three days, followed by oral prednisolone at 1 mg/kg per day with dose tapering. This regimen was effective, and the patient's serum markers were completely normalized in a week after the initiation of the therapy.

Conclusion

We herein report a case of G-CSF-induced aortitis. This adverse event is scarcely reported, but the concept of G-CSF-induced aortitis is recently emerging. Because it seems to appear any patient who has undergone G-CSF therapy, it should be considered in cases of unexplained fever and no treatment response with antibiotics in case of receiving G-CSF therapy. High-dose steroid therapy seems to shorten the disease-affected period in several reported cases. We suggest that the treatment should be started promptly upon diagnosis. Andcontrast-enhanced CT is recommended for long-term follow-up of patients with treated aortitis, particularly for monitoring the subacute or late complications.

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