Congenital Atrophic Plaque

The patient is a 13-year-old female who had had a patchy lesion on her back since birth which increased in size proportional to her age. When she visited our hospital at the age of 13, the lesion was a 30 times 43 mm, slightly depressed, well defined, irregularly shaped, atrophic plaque. Differential clinical diagnoses at that time included macular atrophy, congenital melanocytic nevus, and mastocytosis. Histopathologically, the lesion was characterized by patchy and scattered infiltrates of oval to spindle cells throughout the dermis extending into the subcutaneous fat tissue. Nerve fibers were found in each of the infiltrates. The tumor cells had oval nuclei with relatively abundant cytoplasm and were similar to nevus cells. They were negative for markers such as S-100 protein, neuron specific enolase, epithelial membrane antigen, HMB-45, Leu 7, Desmin, and α smooth muscle actin. However, the histopathological findings suggest that the lesion is a melanocytic or neurogenic tumor, possibly a congenital melanocytic nevus or a cellular neurothekoma, though a definite diagnosis could not be made.     

心腔内粘液瘤的诊治（附18例报告）

心腔粘液瘤１８例，其中左心房粘液瘤１６例，右心房及左心室粘液瘤各１例。所有病例均经超声心动图（ＵＣＧ）诊断，全麻体外循环下胸骨正中切口入路，经房间沟、右房、左房或房间隔切开完成手术。为防止肿瘤组织脱落造成周围血管栓塞，术中除了轻柔的操作，并采用负压抽吸法将瘤体较完整地吸入到心脏切口外针筒内，然后从基底部切除粘液瘤。１８例患者无１例发生手术后栓塞。     

Proinflammatory cytokines in cardiac myxomas.

Serum levels of various cytokines were measured in three patients with cardiac myxomas presenting with and without constitutional symptoms, immunological features and elevated plasma levels of interleukin-6. Interleukin-6 but not other cytokines (interleukin-1, tumour necrosis factor-alpha, interferon-gamma) relate to immunological features of the patients. Circulating levels of atrial natriuretic peptide correspond to haemodynamic changes but not to the tumour-bearing state itself.     

心脏粘液瘤的诊断及外科治疗

我院自１９８１年１１月至１９９３年１０月共手术治疗心脏粘液瘤４２例。其中左房粘液瘤３７例、右房粘液瘤４例、右室粘液瘤１例。全部病例术前均由超声心动图明确诊断。２例术后早期死亡。４０例痊愈出院。本组病例随访无复发。本文就心脏粘液瘤的诊断，手术方法及手术注意事项作了讨论。     

Acute aortic occlusion as an unusual embolic complication of cardiac myxoma

Acute aortic occlusion is an infrequent but dangerous vascular emergency with a mortality rate of 50%,1 resulting from aortic saddle embolus, thrombosis of an atherosclerotic abdominal aorta, or sudden thrombosis of a small abdominal aortic aneurysm. Cardiac myxoma, a benign primary tumor of the heart, accounts for 75% to 80% of cardiac tumors.2,3 Most of myxomas (up to 80%) are localized at the left atrium.4,5 The tumors are typically pedunculated, lobated, and highly mobile with gelatinous a…     

Cardiac myxoma shedding leads to lower extremity arterial embolism: A case report

BACKGROUNDLeft cardiac myxoma (CM) is the most common benign tumor of primary cardiac tumors, but because of its special position caused by pathological physiology change, caused by the complications of the heavier, the surface is often accompanied by blood clots, once fall out, it causes peripheral vascular embolization, such as acute lower limb artery embolization, harmfulness is large, high morbidity, and easy to occur repeatedly.CASE SUMMARYA 67-year-old male patient suddenly appeared numbness and weakness of the left lower limb and could not walk without obvious incentive. The patient was finally diagnosed as left CM complicated with acute lower limb arterial embolism after completing cardiac ultrasound, computer tomography angiography, and histopathological analysis, such as hematoxylin-eosin stain staining, immunohistochemistry and special staining including alcian blue staining and periodic acid schiff staining. Arterial thrombosis was removed successfully by femoral artery thrombectomy, postoperative numbness and weakness of the patient''s left lower limb disappeared, skin temperature became warm, and dorsal foot artery pulsation was accessible. The patient was readmitted to the hospital 8 mo after discharge for left atrial mass resection, and was diagnosed as CM by postoperative histopathological examination. CONCLUSIONAlthough CM is rare, it may be considered as the source of embolism in patients with acute limb ischemia. Repeated loss of thrombus on the tumor and its surface may lead to repeated embolism of peripheral vessels. Cardiac ultrasound is helpful for early diagnosis. Here, we use this case report to highlight left CM as an important cause of acute limb ischemia and to report our experience in the diagnosis and treatment of lower limb arterial embolism caused by CM detachment.     

MRI对胰腺导管内乳头状粘液瘤良恶性的诊断价值

目的 探讨MRI对胰腺导管内乳头状粘液性肿瘤（IPMN）良恶性的鉴别诊断价值。方法 收集2012年1月~2018年6月我院经手术病理证实的IPMN患者24例,均行MRI检查（包括MRI平扫、三期增强以及MRCP）,分析IPMN MRI表现、IPMN良恶性因素,并采用ROC曲线分析IPMN肿瘤最大径及胰管扩张直径与肿瘤良恶性关系。结果 24例IPMN患者中,良性14例,恶性10例。良性与恶性在性别、肿瘤分型、病变位置间比较,差异无统计学意义（P＞0.05）;恶性年龄大于良性,差异有统计学意义（P＜0.05）。IPMN恶性肿瘤最大径为（55.70±10.73）mm,大于良性的（34.20±7.65）mm,差异有统计学意义（P＜0.05）;IPMN肿瘤最大径与肿瘤良恶性关系ROC曲线分析得出:曲线下面积（AUC）为0.87,肿瘤最大径最佳临界值为46.40 mm,敏感度为85.68%,特异性为83.35%。IPMN恶性主胰管扩张最大径为（8.91±3.22）mm,大于良性的（4.82±1.33）mm,差异有统计学意义（P＜0.05）;IPMN胰管扩张直径与肿瘤良恶性关系ROC曲线分析得出:AUC为0.88,胰管扩张最大径最佳临界值为7.35 mm,敏感度为70.00%,特异性为85.73%。结论 MRI能很好显示胰管扩张、囊性病变、管壁内结节等特征,在评估IPMN良恶性中具有敏感性。     

Intramuscular low-grade myxoid neoplasm with recurrent potential (cellular myxoma) of the lower extremity: case report with cytohistologic correlation and review of the literature

"Low-grade myxoid neoplasm with recurrent potential" (cellular myxoma) is a term recently used to describe a subset of soft tissue lesions with histology intermediate between intramuscular myxoma and low-grade myxofibrosarcoma or myxoid malignant fibrous histiocytoma (MFH), while resembling a deeper counterpart of superficial angiomyxoma. Their distinctive biological behavior is characterized by the potential to recur locally, in contrast to intramuscular myxoma, while having no potential to advance in grade or metastasize when compared to low-grade myxofibrosarcoma. We present a cytohistological correlation for an intramuscular location of such a tumor in the lower extremity of a 49-yr-old male.     

Unusual presentation of localized gingival enlargement associated with a slow-growing odontogenic myxoma

Unusual presentation of localized gingival enlargement associated with a subjacent tumoural pathology is reported.The patient was a55-year-old black male,whose chief complaint was a progressive gingival overgrowth for more than ten years,in the buccal area of the anterior left mandible.According to the clinical features and the radiological diagnosis of odontogenic keratocyst,a conservative surgery with enucleation and curettage was performed.Tissue submitted for histopathological analysis rendered the diagnosis of odontogenic myxoma.After 12-month of follow-up,no evidence of recurrence was found.Clinicians should be cautious when facing any gingival enlargement to avoid diagnostic pitfalls and to indicate the appropriate treatment.