Moore Colton M, Loichle Autumn, Tavakolian Kameron, Odak Mihir, Nightingale Savannah, Patel Swapnil V
Internal Medicine, St. George's University School of Medicine, Neptune, USA.
Internal Medicine, Jersey Shore University Medical Center, Neptune City, USA.
Cureus. 2022 Aug 20;14(8):e28198. doi: 10.7759/cureus.28198. eCollection 2022 Aug.
Superior vena cava syndrome (SVCS) is a vascular condition resulting from an impaired venous return to the right atrium. The majority of SVCS cases are caused by mass effect in which extrinsic compression of the vessel leads to obstruction of blood flow. In less common cases of SVCS, thrombus formation and luminal narrowing can result in poor return through the SVC. Inflammatory causes of SVCS are even rarer and poorly documented. IgA nephropathy and rheumatoid arthritis (RA) are two autoimmune diseases with the potential to cause vasculitis, thus increasing the likelihood of intraluminal vessel occlusion. We report a rare case of SVCS in a 65-year-old female with a past medical history significant for atrial fibrillation, IgA nephropathy, chronic kidney disease stage IIIA, and RA who presented with headache, dizziness, and neck pain and swelling extending down the left upper extremity for three days. Inflammatory SVCS is uncommon and cases of SVCS secondary to RA and IgA nephropathy are underreported in the literature thus far. Our hope in presenting this case is to encourage a greater degree of suspicion for vascular complications, such as SVCS, in patients with autoimmune and inflammatory conditions.
上腔静脉综合征(SVCS)是一种由于静脉回流至右心房受损而导致的血管疾病。大多数SVCS病例是由肿块效应引起的,即血管受到外部压迫导致血流阻塞。在较不常见的SVCS病例中,血栓形成和管腔狭窄可导致通过上腔静脉的回流不畅。SVCS的炎症性病因更为罕见且文献记载较少。IgA肾病和类风湿关节炎(RA)是两种有可能引起血管炎的自身免疫性疾病,从而增加了管腔内血管闭塞的可能性。我们报告了一例罕见的SVCS病例,患者为一名65岁女性,既往有房颤、IgA肾病、慢性肾脏病ⅢA期和RA病史,出现头痛、头晕、颈部疼痛以及左上肢向下延伸的肿胀,症状持续三天。炎症性SVCS并不常见,迄今为止,继发于RA和IgA肾病的SVCS病例在文献中报道较少。我们呈现此病例的目的是鼓励对自身免疫和炎症性疾病患者的血管并发症,如SVCS,保持更高程度的怀疑。