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Journal of Clinical Medicine Research

Case Report

Volume 13, Number 12, December 2021, pages 563-566

Acute Epiploic Appendagitis in a COVID-19-Positive Patient With Antiphospholipid Syndrome

Epiploic appendagitis is an uncommon and underdiagnosed cause of acute abdominal pain, affecting about 8.8 per 1 million people per year. Since this condition may be misdiagnosed as diverticulitis or appendicitis, this number is likely an underestimation [1]. It is caused by twisting, inflammation, or thrombosis of the epiploic appendages, predominantly adipose-containing ovoid structures that arise on the antimesenteric serosal surface of the colon connected by a vascular pedicle [2]. Although the presenting symptoms of the condition are nonspecific, patients with epiploic appendagitis most commonly present with localized abdominal pain, more commonly on the left, exacerbated by coughing, deep breathing, or stretching. Nausea, vomiting and loss of appetite are rare symptoms. Patients typically have a normal white blood cell (WBC) count, or mild leukocytosis. Signs and symptoms are self-limiting and rarely last more than one week [3-5]. It is now well-established that high D-dimer levels and procoagulant changes in coagulation pathways are found in patients with severe coronavirus disease 2019 (COVID-19) [6, 7]. This leads to an elevated rate of venous and arterial thrombotic events in this patient population [8-10].

A 50-something-year-old male with systemic lupus erythematosus, antiphospholipid syndrome complicated by chronic lower extremity deep venous thromboses (on coumadin, international normalized ratio (INR) goal 3.5 - 4.5 and inferior vena cava (IVC) filter), chronic pain, chronic obstructive pulmonary disease, paroxysmal atrial fibrillation, myocardial infarction status post percutaneous intervention with two drug eluting stents, hypertension, and hyperlipidemia, presented to our emergency department with chest pain, shortness of breath, and left lower quadrant abdominal pain. Patient’s body mass index (BMI) was 26.9, and he was a current one pack per day smoker with 30-pack-year history.

The patient reported that he had been feeling worsening shortness of breath with non-productive intermittent cough for about one week. The night prior, he awoke from sleeping with new onset of chest pain in the center of his chest, which he described as sharp, non-radiating, 10/10 in severity, and constant. His symptoms persisted over the course of the next couple of hours. He endorsed ongoing generalized headache, subjective fever, ageusia, nausea, vomiting, bloating, severe left lower quadrant abdominal pain, and diarrhea. He stated that the abdominal pain started several days after he noticed the cough and shortness of breath. The abdominal pain was exacerbated by pressure or palpation to the left lower quadrant, and with significant movement. He had not had relief despite pain medications. He denied anosmia, diarrhea, blood in his stool or constipation.

Upon presentation, the patient’s pulse oximeter oxygen saturation (SpO₂) was 99% on 4-L nasal cannula. He was afebrile with otherwise stable vital signs. On physical exam, patient was anxious, breathing comfortably on nasal cannula, abdominal exam positive for diffuse tenderness to palpation, worst in the left lower quadrant, bowel sounds normoactive, abdomen soft and non-distended. Labs were without significant abnormalities (Table 1).

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Table 1. Patient Lab Values

Chest X-ray showed low lung volumes and hypoventilation changes. Computed tomography angiography (CTA) pulmonary embolism (PE) study did not show evidence of acute pulmonary embolism, but did note some mild lung paraseptal and centrilobular emphysema with bilateral dependent atelectasis. The patient was trialed off oxygen, but desaturated to the high 80s with symptomatic shortness of breath. He was self-proned which increased his abdominal pain, and admitted to the inpatient medicine team. Hospital course per respiratory status can be seen below in Figure 1.

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Figure 1. Timeline of respiratory status changes. SFM: simple face mask; HFNC: high-flow nasal cannula; ICU: intensive care unit.

Patient refused self-proning from this time and throughout his hospitalization, due to exacerbation of abdominal pain. Assuming the left lateral recumbent position would typically slightly improve his O₂ saturation if he was desaturating.

Meanwhile, patient continued to complain of abdominal pain, and he underwent computed tomography (CT) abdomen and pelvis on hospital day 2 which showed interval development of a 2.2 × 1.2 cm oval fat attenuation with soft tissue rim along the sigmoid colon mesentery, new since January 11, 2019, consistent with epiploic appendagitis (Fig. 2). A diagnosis was readily established based on clinical presentation, corroborated by CT imaging.

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Figure 2. CT abdomen and pelvis from hospital day 2. The oval fat attenuation with soft tissue rim along the sigmoid colon mesentery is shown as the orange oval. CT: computed tomography.

The acute care surgery team was consulted, who recommended conservative management with an emphasis on pain control. Patient was also placed on 3.375 g of Zosyn for a 7-day course. Despite attempts at pain management with the help of the acute pain service, patient’s abdominal pain continued throughout the course of his hospitalization.

Patient went on to have a 24-day hospital course in total, primarily for the management of his COVID-19 pneumonia. He completed a 5-day course of remdesivir (200 mg loading dose once, following by 4 days of remdesivir 100 mg daily) as well as a 10-day course of dexamethasone 6 mg daily. Throughout this time, he remained on a pain control regimen, but still had unchanged abdominal pain, worst in the left lower quadrant and with palpation. He completed his course of Zosyn. He remained anticoagulated to his INR goal 3.5 - 4.5, for the most part, with the exception of during one episode of epistaxis, and also a large chest wall hematoma during which he suffered significant blood loss. The patient was eventually discharged to a transitional care hospital, on high-flow nasal cannula (HFNC) 40 L/40%, without resolution of his abdominal pain. To the best of our knowledge, the patient has not passed away, although he is not responsive to phone call attempts.

Venous thromboembolism (VTE) is now a well-established complication of COVID-19, and early reports have suggested a VTE rate of approximately 27% in critically ill patients hospitalized with COVID-19 [8]. The high rates of VTE events in hospitalized and critically ill patients with COVID-19 occur despite standard anticoagulant thromboprophylaxis with unfractionated heparin or low-molecular-weight heparin (47/48 in the study of Ren et al and 20/22 in the study of Poissy et al [11, 12]. Some studies, such as that by Llitjos et al have even found that VTE can occur in patients treated with therapeutic anticoagulation from admission [9].

This poses a clinical challenge in deciding the treatment of these patients, given the known and life-threatening risks associated with therapeutic anticoagulation, such as heparin-induced thrombocytopenia, hemorrhagic complications, and heparin-associated osteoporosis. To date, there is no consensus on when and whether or not to provide therapeutic anticoagulation to critically ill COVID-19 patients [13, 14].

Furthermore, it is important to discuss antiphospholipid antibodies (aPLs) and COVID, especially in the case of this patient who had known antiphospholipid syndrome. The causality (if one exists) between aPL and COVID is unclear, although transient aPL elevations have been demonstrated in critically ill COVID patients. Even outside of the setting of COVID, aPL can rise transiently in patients with critical illness and various infections [15, 16]. Other studies have contradicted this finding, showing that aPLs are not elevated in a population of 24 severely ill patients with COVID-19 and VTE [17].

Overall, the studies exploring the relationship between aPL and VTE in the setting of COVID are quite limited and the topic requires further investigation. Elucidating the pathophysiology of VTE in the setting of COVID will lead to the more appropriate treatment and decrease in morbidity and mortality associated with this complication [18].

Epiploic appendagitis is an underdiagnosed and rare cause of acute abdominal pain. It can be caused by venous thrombosis, and should be considered in COVID-positive patients with abdominal pain, despite anticoagulation. Epiploic appendagitis has not yet been diagnosed as a known complication of COVID-19, and therefore its incidence and prevalence in these patients is unknown. Putting epiploic appendagitis on the radar as a cause of abdominal pain in COVID-19 patients has the potential to aid diagnosis, and to avoid misdiagnosis of the condition, avoiding clinical mismanagement in this patient population. Elucidating the causal factors for VTE in COVID-19, inside and outside of aPL will add to our understanding of the pathophysiology of COVID-19 and its complications, leading to improvements in our medical management of these deathly complications.

Acknowledgments

None to declare.

Financial Disclosure

The authors have no relevant financial interest to disclose. The authors did not receive any support from any organization for the submitted work.

Conflict of Interest

Case abstract was presented as a poster at the 2021 SGIM Northwest & California-Hawaii Virtual Regional Meeting.

Informed Consent

Verbal informed consent was obtained from the patient.

Author Contributions

All authors have contributed substantially to the conception of the work, the drafting or revising of the work, have approved the final work to be published, and agree to be accountable for all aspects of the work. Dalia Kaakour was the lead in conception of the case report, as well as the primary author of this manuscript. Priyanka Teckchandani was involved in the conception of the case report, took part in writing portions, as well as significantly edited portions of this case report. Huawei Dong was also involved in conception of case report, and was editor.

Data Availability

The data supporting the findings of this study are available from the corresponding author upon reasonable request.

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