Orbital hydatid cysts: Report of four cases

Hydatid cysts of central nervous system are rare and comprise only 2% to 3% of all hydatid cysts reported. Orbital localization is very uncommon and has been reported less than 1 % of all hydatid diseases. The primary treatment of hydatid disease is surgical. The most important complication of the surgical treatment is secondary hydatidosis due to spillage of the cyst contents. Because of the difficulties of the orbital localization, total extirpation of the cysts without rupture is almost impossible. Preventing spontaneous rupture of the cysts during surgery and postoperative antihelmintic treatment should be taken into consideration in these cases.This study includes four cases who underwent surgery for orbital hydatid cysts. Radiological characteristics, operative technique and postoperative medical therapy are discussed.     

GROWTH DISTURBANCES ASSOCIATED WITH UNTREATED BENIGN BONE CYSTS

Background: The occurrence of benign bone cysts adjacent to an active physis may be associated with a physeal arrest. That arrest may result from physeal penetration of the cysts itself, secondary pathologic fracture or the result of surgical curettage. Methods : The pre-treatment X-rays of patients attending the Bone Tumor Clinic at the Children's Hospital and Medical Center were reviewed. Those patients presenting with a bone cyst were identified and the affected side was compared to the normal side in order to determine growth discrepancies. Results: Three cases of benign bone cysts are presented that were located adjacent to a growing physis and produced growth disturbance in the absence of surgical intervention. Conclusions: The risk of growth disturbance in itself should not be a contraindication to surgical intervention.     

颅内表皮样囊肿的常规T_1WI、T_2WI、FLAIR及DWI对比分析

目的:通过定性分析和定量比较来探讨颅内表皮样囊肿(ECs)的FLAIR和DWI特征。方法:ECs16例,测量其T1WI、T2WI、FLAIR及DWI上病灶信号强度和ADC值,计算组织间对比度(CR)和对比噪声比(CNR)。结果:在FLAIR上ECs平均信号强度高于脑脊液(CSF),低于脑组织。在T1WI上,表皮样囊肿与脑脊液间的CR和CNR分别是0.11±0.06和1.02±1.11;在T2WI上,ECs与CSF间的CR和CNR分别是0.05±0.04和1.05±0.58;而在DWI上,ECs与CSF间的CR是12.56±2.87,CNR是18.23±5.42。16例患者示踪DWI图像上均呈明显高信号。ECs平均ADC值明显低于CSF(P<0.001),而高于脑白质(P=0.002)。结论:FLAIR对颅内表皮样囊肿显示优于常规MRI序列,DWI描述ECs轮廓优于其它MRI序列。     

Developmental odontogenic cysts. An update1

This review paper reports recent advances in the subject of developmental odontogenic cysts, essentially those of the past decade, starting with reference to the new WHO classification (1). On keratocysts, the latest reported recurrence rates are assessed as are their mode of growth, immunocytochemistry, immunology, genetic studies, and work on specific keratocyst antigens. There is a critical account of the group of lesions which includes the gingival cyst of adults, lateral periodontal cyst, hotryoid odontogenic cyst and glandular odontogenic cyst, and their possible relationship to one another. On dentigerous cysts, reference is made to the relationship between them and deciduous teeth, as well as to their immunocytochemistry and immunology. Recent work on the unicystic ameloblastomas. their classification and prognosis, is assessed, as is the calcifying odontogenic cyst and its relationship with solid odontogenic tumours.     

骨巨细胞瘤继发动脉瘤样骨囊肿的影像诊断

目的提高骨巨细胞瘤（GCT）继发动脉瘤样骨囊肿（ABC）的认识和影像诊断水平。方法搜集经手术病理证实的12例GCT继发ABC的X线、CT、MRI和病理学资料，分析和总结其影像征象。结果12例中6例病变发生于长管状骨，6例发生于盆骨。12例病变X线均表现为囊状膨胀性溶骨性骨破坏，10例呈偏心性破坏，2例为中心性破坏；4例病灶内出现骨性分隔，6例骨皮质中断，4例出现软组织肿块，有明显硬化边者2例。10例行MR平扫和增强检查，均呈多囊的囊实性膨胀性肿块，8例为边缘性实性结节，2例为实性基础上的广泛囊变，全部患者均可见多个液一液平面，7例出现软组织肿块；1例肿块内可见局灶性含铁血黄素沉着。8例行螺旋cT平扫、增强、CT血管成像（CTA）和三维（3D）多平面重组（MPR），病变显示为囊实性肿块，骨皮质破裂并形成软组织肿块5例，6例肿块内出现液．液平面，全部肿块实质性部分和囊壁明显强化，囊性部分不强化，3例肿块内可见增粗迂曲的供血动脉，未发现动静脉畸形。12例手术所见和术后病理显示肿块均由多发含血的囊腔和实性部分组成，病理诊断结果均为GCT伴发ABC，其中Ⅱ级GCTl0例，Ⅲ级2例。结论GCT伴发ABC并不少见，充分理解其病理组织学基础，并选择恰当的影像检查方法（X线＋MRI或X线＋CT）对其正确诊断非常重要。     

成人先天性肺内支气管囊肿的影像学诊断

目的:探讨成人先天性肺内支气管囊肿在CT、MRI表现上的特征。方法:37例经手术及病理证实的肺内支气管囊肿;男25例,女12例,年龄18～63岁,平均35岁。均行X胸片,24例行CT平扫及增强扫描,13例行MRI检查。结果:分布在右肺16例,左肺21例。形态以圆形为主,可以呈葫芦状、长条状或不规则形。22例囊肿含有液体,8例含气体,6例含有气液面,4例含有曲菌球,囊壁钙化7例,呈点状和弧线状。囊壁见有轻-中度强化,其中以含液囊肿较明显,囊肿周围气肿15例。结论:大部分成人先天性肺内支气管囊肿的CT、MRI表现有一定的特征,有助于术前诊断。     

Chronic renal failure and its treatment in tuberous sclerosis

BACKGROUND.: Chronic renal failure is rare in tuberous sclerosis, but itsprecise frequency is not known and treatment modalities havenot been evaluated. METHODS.: A questionnaire was addressed to the 260 French dialysis centresand the characteristics of 65 patients with tuberous sclerosisand chronic renal failure were analysed. RESULTS.: In France the approximate prevalence of tuberous sclerosis withend-stage renal failure is 0.7 cases per million and that ofend-stage renal failure in tuberous sclerosis 1 per 100. Tuberoussclerosis with chronic renal failure was more frequent in females(63.1%) and was diagnosed at a mean age of 29 years. Renal impairmentwas the first manifestation of tuberous sclerosis in about halfthe cases. Renal tumours were frequent, with angiomyolipomasin 15 cases (23.1%), cysts in 12 cases (18.5%), and both in35 cases (53.8%). Malignancies were associated in nine cases(13.8%). Nephrectomy was done before dialysis in 21 cases (32.3%),and after the start of dialysis in six cases (9.2%). All butone of the 48 patients with end-stage renal failure were treatedby dialysis; 20 were transplanted, with good results. CONCLUSIONS.: Tuberous sclerosis with end-stage renal failure is rare. Thesepatients require dialysis and renal transplantation, but werecommend binephrectomy after starting dialysis and before transplantation,given the risk of cancer and bleeding related to angiomyolipomas.     

The development of post-traumatic cyst-like lesions in bone

Cyst-like lesions in the radius and tibia were observed in two children as a post-fracture event. The pathogenesis of these lesions is discussed. Cut sections from anatomic specimens display extensive hemorrhage in subperiosteal as well as endosteal and trabecular bone. Cysts arising from hemorrhagic resorption in various locales may explain the occasional atypical appearance of these lesions.     

First branchial cleft fistula presenting with external opening on earlobe

First branchial cleft fistula is a rare congenital malformation of the head and neck with an incidence of less than 10% of all branchial cleft defects. We herein report a 15-year-old girl who had a cystic mass in the postauricular region with an external opening on the posterior face of the earlobe. Surgical exploration revealed that a second sinus tract was passing through the conchal cartilage without going beyond the skin of the external acoustic meatus. The mass and the tract were excised along with the opening on the earlobe as well as the skin island surrounding the opening. The case was treated surgically with success .The significance of our case was the location of external opening on the earlobe.     

Clinical and radiographic features of simple and hydatid cysts of the liver

The advances of hydatid chemotherapy and the non-operative management of simple (epithelial) hepatic cysts make a correct diagnosis of increasing importance. Twenty-six patients with hepatic hydatid cysts and eleven with simple cysts were reviewed. In both groups clinical presentation was most frequently due to pain. Sex, age and size of the cysts were similar. Hydatid serology was negative in six of the hydatid patients (23 per cent). None of the simple cyst patients had positive serology but one had a borderline titre. Ultrasound and computerized tomography identified daughter cysts within the main cyst in only 17 hydatid cysts (65 per cent) and considerable intra-cyst debris was also present in five of the simple cysts. Seven of the simple cysts were deroofed surgically and the remainder underwent percutaneous aspiration. Sixteen of the hydatid cysts were found to have a biliary communication whereas this was not found with any simple cyst. The difficulties in making a precise diagnosis in some patients with a liver cyst should deter the interventional radiologist and restrain the hydatid chemotherapist.