Jarcho-Levin syndrome is a rare central skeletal system defect with the involvement of ribs and vertebrae and association of short trunk stature and some other organ anomalies. One of the common problems is different rate of respiratory abnormalities. Chest X-Ray is the primary base for the diagnosis, but spiral 3D CT scan give us more accurate evaluation of the ribs situation. There are also c...

هدف: معرفی یک بیمار با همانژیوم کاورنوس (CH) در پلک تحتانی. معرفی بیمار: آقای ۳۷ ساله‌ای با شکایت از یک توده قابل لمس و بدون درد در پلک تحتانی راست از ۲ سال قبل به بیمارستان لبافی‌نژاد مراجعه نمود. وی تغییر اندازه توده را با فعالیت ورزشی و تغییر وضعیت بدن و یا مانور والسالوا ذکر نمی‌کرد. در معاینه، کاهش دید، پروپتوزیس، اختلال حرکت عضلات خارج چشمی و دوبینی وجود نداشت. در CT اسکن، توده‌ای لوبوله ...

سابقه و هدف: شیلوتوراکس که در اثر نشت لنف به فضای پلور ایجاد می شود. در دوره نوزادی نسبتا نادر است، به دو شکل مادرزادی و ایاتروژنیک (Iatrogenic) حادث می شود. گزارش مورد: نوزاد دختری است که از مادر 30 ساله به روش سزارین متولد شد. در سن 7 روزگی به علت دیسترس تنفسی و سیانوز در بخش NICU بیمارستان کودکان امیرکلا بستری شد. عکس ریتین کدورت یکنواخت قفسه صدری راست همراه با شیفت مختصر قلب و مدیاستین به س...

When abdominal and thorasic organs are inversed it is called situs inversus and when most of the these organs are positioned abnormally and heterogenic It is called situs ambigus (Heterotoxy syndrome) which is a rare congenital defect (Incidence 1.44 in 100/000 live birth) In these, abnormal organs shift which could be to the Right side or left side (Right Isomerism, Left Isomerism). One of the...

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Sarcoidosis, a multysystem granulomatous disease, begin most frequently in people between 20 and 40 years old. The etiology is unknown, but alteration in the Immune system are clearly involved in its pathogenesis. Organ involvement is usually asymptomatic, and the disease most frequently regress spontaneously, but it may progress to a more chronic state of fibrosis with sever functional impai...

Primary sarcomas of the fallopian tube are extremely rare and excluding malignant mixed mullerian tumors, 34 cases have been reported in the literature of the recent 100 years. Out of 34 cases only 15 cases have clearly been described as leiomyosarcomas. The patient of the present report was a 45-year-old woman with leiomyosarcoma confined to the right fallopian tube. She is still a...

Mesenchymal chondrosarcoma(MC) was first described in 1959. MC is a rare tumor arising in bone or soft tissue which is composed of well differentiated cartilage with in a proliferation of primitive mesenchymal cell. MC occurs most often in the second and third decades of life. The prognosis is poor, local recurrence and metastases are frequent. A 32 year old, white female consulted a ...