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Bartholin’s Gland Bilateral Nodular Hyperplasia: A Case Report Study
Bartholin’s Glands Hyperplasia Adenoma
2015/10/13
Introduction:: Tumors which originate from the Bartholin’s glands (BGs) are very rare. Many solid masses that arise from the BGs are carcinoma, though these benign solid lesions are rare.
Isolated Renal Mucormycosis after Liver Transplantation:An Unusual Case Report
Kidney Mucormycosis Liver transplantation
2015/9/25
Mucormycosis is a rare complication of immunosuppression. Most of the reported cases have been rhinocerebral or disseminated. Isolated renal involvement is extremely rare and until now less than 30 pa...
Primary Splenic Hodgkin’s Disease in a Patient with Chronic Granulomatous Disease,a Case Report
Chronic granulomatous disease Spleen Hodgkin’s disease
2015/9/21
Here we report a 20-year-old male, a known case of chronic granulomatous disease (CGD), who presented with fever and splenomegaly. After splenectomy, primary splenic Hodgkin’s disease was diagnosed. I...
Nevoid Basal Cell Carcinoma (Gorlin) Syndrome (Case Report)
Nevoid basal cell carcinoma Gorlin syndrome Keratocyst
2015/9/21
A16 year old boy was admitted to the hospital because of a swelling on the left side of mandible .He had multiple small indurated pearly papules on the head and neck with multiple well circumscribed r...
Ohtahara syndrome and IVF:A case report
Ohtahara syndrome Early infantile epileptic encephalopathy ، In vitro fertilization Suppression burst Cerebral dysgenesis Hemimegalencephaly Intractable seizures
2010/1/4
Ohtahara syndrome or ealy infantile epileptic encephalopathy is a rare cause of epileptic seizures during infancy and represents the earliest type of age related symptomatic generalized epilepsies. Th...
Familial occurrence of lip pits:A case report
Lip pits deformities autosomal dominant trait
2009/12/24
Lip pits are among the rarest congenital deformities recorded. Initially reported in 1845, it’s familial occurrence has been reported just once. These developmental anomalies occur either as an isolat...
Cyclosporine-induced reflex sympatethic dystrophy syndrome in a patient with graft versus host disease after bone marrow transplantation: a case report
Cyclosporine bone marrow transplantation reflex sympathetic dystrophy syndrome
2009/12/17
Background: Reflex Sympathetic Dystrophy Syndrome (RSDS) is a rarely described complication which characterized by pain, edema, movement and vasomotor disorders, trophic changes in the skin and patchy...
Using Paradox in Family Therapy among Iranian Families: A Case Report
Couple therapy Family therapy Iran Methods
2009/12/7
Objective:
This study assessed the effect of paradox in family therapy.Paradox, as a therapeutic tool, has been developed by a number of therapists,especially Mara Selvini Palazzoli.
Method: Th...
Retroperitoneal Leiomyosarcoma of the Inferior Vena Ca-va: A Case Report
Retroperitoneal Leiomyosarcoma Inferior vena cava
2015/9/18
Leiomyosarcoma of the inferior vena cava (IVC) is a rare sarcoma, but it is the most common primary malignancy of the IVC. It has an extremely gloomy prognosis. We describe a 40 year-old white female ...
PagetÕs disease of the breast is a rare condition with an incidence of 1-4.3% of all mammary malignancies. Of all malignant breast cancers, 1% occur in male patients, and thus PagetÕs di...
A Case Report of Ecstasy-induced Acute Hepatic Failure
Ecstasy toxic hepatitis 3,4-methylenedioxymethamphetamine MDMA
2009/6/19
3,4-Methylenedioxymethamphetamine (MDMA),also known as "ecstasy", is a synthetic, psychoactive drug chemically similar to the stimulant methamphetamine and the hallucinogen mescaline. It can cause cog...
Primary retroperitoneal seminomas account for approximately 2% of all seminomas. Despite the availability of ultrasonic examination, differentiating the primary retroperitoneal tumor from a metastatic...
Background: Lethal toxic encephalopathy of shigellosis (Ekiri syndrome) is a rare complication of the shigella infection presented with fever, severe toxicity, seizure and diffuse brain edema, coma an...
The incidence of anomalies is high in multiple gestations especially in monochorionic twins. This paper reported a case of an acardiac parabiotic twin, a rare deformed fetus which occurs typically in ...
Congenital chloride diarrhea:a case report
Congenital chloride diarrhea Metabolic alkalosis Hypochloremia
2010/4/12
Objective: Congenital chloride diarrhea (CCD) is a rare autosomal recessive disorder of intestinal chloride absorption. Pathognomonic features consist of watery diarrhea, failure to thrive, dehydratio...