amyloidosis

As the name implies, this form of amyloidosis is inherited. This type often affects the liver, nerves, heart and kidneys.

Researchers are studying several therapies to determine their place in the treatment of amyloidosis.

and that of localized amyloidosis was observation or localized excision .

Among the heredofamilial forms of amyloidosis, only the Portuguese neuropathic type has so far been studied in any detail.

The final diagnosis was a rare, isolated pulmonary diffuse alveolar-septal form of amyloidosis.

Amyloidosis is a broad and complex class of diseases that comprises several etiologies, many manifestations, and a diversity of outcomes.

The severity of amyloidosis depends on which organs the amyloid deposits affect.

This article reviews the research status of pathogenesis and diagnosis as well as the treatment of dialysis related amyloidosis.

Traumatic purpura occurring in colloid milium may be analogous to that occurring in systemic amyloidosis.

In search of a second opinion, Poblete tracked down amyloidosis experts on the Internet.

Objective: To explore the clinical and histopathological characteristics of secondary renal amyloidosis.

This report presents a case of systemic amyloidosis involving the stomach and rectum.

INTRODUCTION: Amyloidosis is characterized by extracellular deposits of proteins.

Objective: To explore the clinical characteristics and pathogenesis of primary systemic amyloidosis.

Localised amyloidosis is a rare lesion of the upper aero-digestive tract, predominating in the larynx.

Congo red stain has been performed on the myocardium in a case of amyloidosis.

In recent years, kidney, heart, skin, throat and bladder amyloidosis are reported, while hepatic amyloidosis is rarely reported.

The place of this drug cannot yet be properly assessed in the management of human amyloidosis.

The suitability of regular dialysis or renal transplantation for patients with amyloidosis therefore arises.

And when amyloidosis affects the electrical system of your heart, this may disturb your heart's rhythm.

OBSERVATION: A 66 year-old patient presented with a pseudo-tumoral amyloidosis of the cavum.

Though there's no cure for amyloidosis, treatment may help manage signs and symptoms and limit further production of amyloid protein.

The signs and symptoms of amyloidosis are often vague and mimic those of other conditions, so it can be difficult to diagnose amyloidosis.

Objective To improve the diagnostic rate of local amyloidosis of stomach.

Despite these approaches to treatment, death in uraemia remains a common outcome in renal amyloidosis.

In systemic amyloidosis positive biopsies have been obtained from a variety of sites(Table 3).

Amyloidosis. This disorder occurs when substances called amyloid proteins accumulate in your organs.

When amyloidosis affects your heart, a common symptom is shortness of breath, even with slight exertion.

Objective: To improve the diagnostic competence for amyloidosis of larynx both clinically and radiologically .

and myocardial biopsy, for identifying infiltrative diseases such as myocarditis, amyloidosis, hemochromatosis, and sarcoidosis.

Methods To analyze the clinical and laboratory features in 5 cases of the primary systemic amyloidosis.

Claims have been made for clinical improvement in amyloidosis after treatment with dimethylsulphoxide(24)(25).

Amyloidosis, a disease where abnormal proteins are deposited in tissues, can occur in CD.

Hepatic amyloidosis is a part of systemic amyloidosis.

Objective To explore CT findings and clinical value of cerebral hemorrhage caused by cerebral amyloidosis angiopathy(CAA).

This is characteristic for amyloid. Amyloidosis is a cause for " infiltrative " or "restrictive" cardiomyopathy.

Family history. Some cases of amyloidosis are inherited.

Still running the new biopsy for amyloidosis?

Has anyone in your family ever been diagnosed with amyloidosis?

Method: Reviewed 4 cases of primary amyloidosis of the bladder in our hospital.

The exact cause of primary amyloidosis is unknown, but doctors do know that the disease begins in your bone marrow.

Age. The majority of people who develop amyloidosis are older than 60.

Objective: To study the epidemiology, manifestation, diagnosis and treatment of primary tracheobronchial and pulmonary amyloidosis.

Signs and symptoms of amyloidosis depend on which of your organs are affected. When signs and symptoms are evident, they may include:

A case of chronic lymphocytic leukemia complicated by membranous nephropathy and amyloidosis

A case of primary macroglobulinemia complicated with psoriasis and renal amyloidosis

Clinical and pathological manifestations of light chain nephropathy and primary amyloidosis

Imaging Features and Clinical Situations of Primary Tracheobronchial Pulmonary Amyloidosis

Caring Patients with Primary Tracheaebronchial Amyloidosis after Interventional Therapy through Bronchoscope

Clinicopathological and diagnostic study of amyloidosis of oral maxillofacial area

Ultrastructural and immunoelectron microscopic study on light chain deposition diseases and primary amyloidosis of the kidney

The clinicopathological and diagnostic study of lingual amyloidosis

A Case of Nodular Localized Primary Cutaneous Amyloidosis

Primary hepatic amyloidosis: report of 4 cases and reviews of the literature in and abroad

Analysis of Clinical Manifestations of Pharyngeal and Laryngeal Amyloidosis

Clinical investigation of dialysis- related amyloidosis

Ultrastructural observation and analysis of renal amyloidosis

Clinical analysis of secondary amyloidosis after rheumatic disease

Pathological analysis of the renal amyloidosis

Clinical Characteristics of Seven Cases of Cardiac Amyloidosis

Treating primary systemic amyloidosis

Treating secondary amyloidosis

Anyone can develop primary amyloidosis, but certain factors place you at greater risk:

The pathogenesis and treatment of secondary renal amyloidosis

Clinical and pathological features of renal amyloidosis

Clinical Value of Lingual Biopsy in Diagnosis of Primary Systemic Amyloidosis

The clinical report of dialysis - related amyloidosis

Primary Tracheobronchial Amyloidosis 10 Cases Treated with Bronchoscopy Nd: YAG

Diagnosis of Cutaneous Amyloidosis by Rapid Stain with Methyl Violet

The Clinical Analysis and Diagnosis of Cardiac Amyloidosis

Primary circumscribed amyloidosis of skin

Heart, Lung, and Blood Research - Light chain amyloidosis

Radiographic Findings of Amyloidosis in Thorax(A Report of 3 Cases with Review of Literatures)

Nursing care of patients with primary systemic multiple organs amyloidosis

Diagnosis of Amyloidosis of Larynx

How to prevent dialysis - related amyloidosis