Intravascular fasciitis involving the external jugular vein and subclavian vein: A case report

INTRODUCTION

Intravascular fasciitis (IVF) was first proposed by Patchefsky[1] in 1981 as a special type of nodular fasciitis involving the small and medium veins or arteries. The disease is rare and rarely reported domestically or internationally. Intravascular fasciitis is a variant of nodular fasciitis, which is caused by the reactive intravascular proliferation of myofibroblasts. The histology of IVF is very similar to that of typical nodular fasciitis, but it often involves the layers and lumens of blood vessels,frequently leading to an overdiagnosis of vascularized malignancies[2,3]. IVF most commonly occurs in the upper extremities, head and neck, followed by the lower extremities and trunk, but there have been reports of rare sites, such as the mouth and maxillofacial region[4-7]. This study reports intravascular nodular fasciitis of the external jugular vein and subclavian vein and explores its clinical and pathological features, diagnosis and differential diagnosis combined with a literature review to raise awareness of rare lesions and avoid misdiagnosis.

CASE PRESENTATION

Chief complaints

A 13-year-old boy came to our clinic with his parents due to a mass on the left side of his neck for 1 mo.

History of present illness

我二話不說就答應了。我拿針在窗戶上戳了個小孔，然后站在槐樹上。別呦呦在屋里寫字，若我能說出她寫的是什么字，我就“無罪”了。

History of past illness

The patient had been in good health until he showed evidence of the disease.

Personal and family history

The patient was not from a consanguineous marriage and there was no family history of similar disease.

Physical examination

November 14, 2020

Laboratory examinations

The results of laboratory examinations on admission were normal, including routine blood and coagulation function tests, liver and kidney function tests, tumor markers,urine tests and stool tests.

Imaging examinations

Grade B (Very good): 0

The pathologist reported that the mass was a spindle cell mesenchymal tumor without definite malignant features, but the specific tumor type and nature needed to be determined by routine histology and immunohistochemistry. Surgery was then performed; because only the mass was removed, no vein reconstruction was required.

興趣是數(shù)學創(chuàng)造的重要動力之一，興趣是力求探索，獲得數(shù)學創(chuàng)造的帶有情緒色彩的意向活動。學生對數(shù)學的迷戀往往是從興趣開始的，由興趣產(chǎn)生動機，由動機到探索，由探索到成功，在成功的快感中產(chǎn)生新的興趣和動機，推動學習的不斷成功。

Pathologic examination was based on a microscopic investigation, which reported that the mass from the left jugular vein was a fibroblast/myofibroblast tumor,consistent with intravascular nodular fasciitis. Hematoxylin-eosin staining showed that the mass was composed of spindle cells, which were mainly fibroblasts and myofibroblasts. The cell morphology was relatively consistent, with an irregular fascicular-shaped arrangement. The atypia was mild, with a small amount of nuclear division, a small amount of mucous degeneration and collagen deposition in the stroma, as well as scattered inflammatory cell infiltration and erythrocyte extravasation (Figure 2). Immunohistochemistry studies showed that the spindle cells were positive for vimentin, caldesmon and smooth muscle actin and negative for S-100 protein, desmin, CD34, and c-kit; Ki-67 staining revealed a low proliferative index (5%-10%), confirming their myofibroblastic differentiation (Figure 3). The USP6 rearrangement test was also positive (Figure 3). Overall, the results were consistent with IVF.

克里斯蒂娜亂舞著胳膊，沖著護欄的位置摸索。沒有別人為她打氣，只有艾爾用一雙大手在嘴邊括成喇叭狀大喊著鼓勵她，他的眼睛緊緊盯著克里斯蒂娜的雙眼。我多希望自己也能給她打氣，我多希望自己能沖上去幫她，可我只是一動不動地站在原地盯著她，同時納悶這種討厭的自私自利到底存在多久了。

FINAL DIAGNOSIS

Left external jugular vein and subclavian vein IVF.

TREATMENT

Conservative treatment of this disease has a certain cure rate, so both clinical observation with conservative treatment and surgical treatment options are available for this disease. Surgical indications were present in this patient, and the surgical treatment option was selected by the patient and his family. Therefore, the patient underwent left neck mass resection after the relevant examinations. After surgical treatment, he had no neurological symptoms or swelling of his arm.

The surgery began with an 8 cm skin incision that was made along the left supraclavicular vein, and the solid mass in the external jugular vein was visible on the deep surface of the left supraclavicular platysma muscle. The solid mass, approximately 4 cm long, grew along the blood vessel and involved the left subclavian vein and its surrounding branches. As requested by the patient's family members, no claviculectomy was performed during the operation. Only the external segment of the jugular vein and the mass in the accessible superficial branch segment were completely removed. Considering that the mass could be malignant and that there was a possibility of extensive excision, a piece of tissue was sent for rapid frozen pathology.

OUTCOME AND FOLLOW-UP

The patient had no thoracic duct injury or pneumothorax after the operation and was discharged four days after the operation. The outpatient review was good one month after discharge. Through telephone follow-up one year after discharge, the patient noted that the left neck did not have a lump or discomfort. The next follow-up will be two years after discharge. The disease will be mainly monitored for potential malignant behavior.

DISCUSSION

Nodular fasciitis is a nonneoplastic myofibroblastic hyperplasia that grows quickly, is sometimes rich in cells and has certain atypicality. This condition can be seen with a high number of mitotic figures and is easily misdiagnosed as various types of soft tissue sarcoma; therefore, it is also known as pseudosarcoma fasciitis. IVF is a rare and special type of nodular fasciitis; thus far, only seven cases have been reported in the domestic literature, and thirty-six cases have been reported internationally. IVF generally occurs in adolescent and young adult patients, with an average age of onset of 26.5 years worldwide. Of these thirty-six patients, 80% were under the age of thirty.There is no significant difference in the incidence rate between males and females, and the ratio is close to 1:1[8-10]. However, among the cases reported domestically, the epidemiological characteristics are inconsistent with those of foreign cases, which may be caused by an insufficient number of reported cases. Usually, before the onset of the disease, the patients were healthy, and even after disease development, the patients generally had no feelings of discomfort, such as pain, tenderness or decreased mobility. IVF is most commonly found in the upper extremities, head and neck,followed by the lower extremities and trunk, and there have been reports of rare sites[5-7]. Most of the clinical manifestations have been painless masses that grow slowly under the skin. A few may have pain or tenderness. Most of the lesions were solitary nodules, and a few patients presented with multiple nodules, the size of the lesion ranged from a minimum of 0.6 cm to 5 cm, and the course of the disease ranged from 2 wk to 8 years[11]. IVF is a benign disease that is usually cured by simple local excision.Thus far, the pathogenesis of endovascular fasciitis is still unclear. It was confirmed that spindle cells are derived from myofibroblasts based on their immunohistochemical characteristics. A few cases have suggested that this condition may be related to previous trauma, thrombosis, and high levels of estrogen[12].

IVF mainly involves small veins or arteries, where lesions extend longitudinally along the vessels and pass through the vessel wall into surrounding connective tissue and adjacent vessels. Due to the small size of the vessels, the lesions may have a polynodular appearance, and intracavitary lesions are separated from the main tumor.The histological features are myofibroblast proliferation with a fractured structure,erythrocyte exosmosis, and a mucous background, but interstitial mucous degeneration is not evident, and there is no pleomorphism and rarely mitosis[6,7]. The intravascular component of IVF can be identified by immunohistochemical staining for elastin and smooth muscle actin. Immunohistochemical staining for smooth muscle actin, caldesmon and vimentin indicates positivity for spindle cells, Ki-67 staining reveals a low proliferative index (< 10%), and staining for c-kit, S100 protein, desmin,CD31 and CD34 is negative, suggesting that IVF involves myofibroblastic differentiation[5,11].gene rearrangement has been recently demonstrated in nodular fasciitis, and the presence of fusions involving thegene in most cases provides a useful tool for diagnostic confirmation[13,14]. Because of its vessel involvement, IVF may be mistaken for a malignancy. When IVF cells undergo atypical changes, more mitotic signs may occur, often involving various layers and lumens of blood vessels,which may lead to the overdiagnosis of malignant tumors, such as fibrosarcoma,leiomyosarcoma, and mucinous liposarcoma. Despite the invasive growth of these lesions, there is no evidence of invasive clinical behavior, recurrence or metastasis[7].The absence of large atypical hyperchromatic nuclei, and the presence of abnormal mitotic figures and immunohistochemical characteristics of the spindle cells can identify IVF[11,15].

CONCLUSION

Intravascular fasciitis is a rare vascular-associated nodular fasciitis that is easily misdiagnosed as other tumors. We report a case of this rare disease and provide insights on IVF, with the hope of improving the recognition of non-neoplastic lesions to avoid misdiagnosis.

We thank all the histology technologists at the Department of Pathology, Hangzhou First People's Hospital for their technical support.

選用于2016年1月至12月期間在本院接受糖尿病治療的100例患者作為研究對象進行分析,并根據(jù)其實施品管圈活動前后,將其平均分成兩組,即觀察組(實施品管圈活動后)與對照組(未實施實施品管圈活動)。在觀察組中,患者中,男性27例,女性23例;年齡55~70歲不等,平均年齡68.25±1.05歲,病程1~10年不等,平均年齡5.68±0.67年。在對照組患者中,男性26例,女性24例;年齡56~71歲不等,平均年齡68.52±1.20歲;病程1~11年不等,平均年齡5.57±0.54年。對比兩組的年齡、性別等臨床資料,其差異甚小,存在統(tǒng)計學意義(P>0.05),具有可比性。