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ERITROPOIESIS DAN ASPEK UMUM ANEMIA By: Cut Indriputri Trisna Bayu. APA ITU HEMATOPIESIS.. HEMATOPIESIS LEUKOPOIESI LIMFOPOIESIS. Eritropoesis meningkat. Defisiensi Besi YANG MEMPENGARUHI MENINGKATKAN: 1. Glutation 5. Vit. C 4. Besi bentuk Ferro 2. Besi Anorganik 3. Eritropoiesis Pada Sumsum Tulang – Download as Powerpoint Presentation .ppt /.pptx), PDF File .pdf), Text File .txt) or view presentation slides online.

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Intestinal metaplasia with dysplasia of the gastric corpus-fundus mucosa and hyperplasia of chromaffin cells, which are typical eritopoiesis of late-stage autoimmune gastritis, are considered precursor lesions.

CDK Edisi 270 – Neurologi

Sumsum tulang normal dapat meningkatkan kemampuan eritropoiesisnya kali lipat. In addition to old age, mutations also cause congenital protein misfolding disorders. The concepts involved in the detection and characterization of B cell lymphoproliferative processes are revisited in this paper by identifying parameters that, when analyzed appropriately, are both necessary and sufficient. The objective of this analysis was to investigate prognostic factors that influence the outcome of Epstein-Barr virus EBV -related posttransplant lymphoproliferative disorder PTLD after a rituximab-based treatment in the allogeneic hematopoietic stem cell transplant HSCT setting.

After administration of 80 mg methylprednisolone, neurologic symptoms disappeared within 24 h and aralah patient fully recovered. Dalam beberapa menit pasien akan sesak nafas, demam, nyeri pinggang, menggigil, mual, muntah, dan syok. In leukemia the most common imaging pattern is diffuse enlargement. We have previously shown that myxoma virus specifically targets various human solid tumors erirropoiesis leukemia cells in a variety of animal models, while sparing normal human or murine tissues.

Meaning of “ginjal” in the Malay dictionary

The year-old man was initially misdiagnosed with ulcerative colitis UC. In the present article, we show the epidemiological, clinical, and histopathological aspects, as well as the treatment of these two viral diseases that are very similar, being differentiated only by their epidemiological aspects.


Thus, it eeitropoiesis almost irresistible to describe phenomena in numerical terms or by ‘ratios’ that have the appearance of ‘accuracy’ due to the presence of numbers obtained from thousands of cells. Although chemotherapeutic strategies such as CHOP have been often selected, they have exhibited only limited efficacy. We present one such case. Nilai normal dan stabil akan dicapai pada hari ke sampai hari ke This specific property of the A3 antigen points to its significance for diagnostics and malignancy staging of lymphoproliferative disorders.

To test the autoimmune reactivity of the fish skin, the participants were tested with the following ELISA enzyme-linked immunosorbent assay tests: Most infected people maintain an asymptomatic but persistent EBV infection lifelong.

Given the specific target of this aggression, autoimmune gastritis is typically restricted to the gastric corpus-fundus mucosa. Lymphomatoid granulomatosis is a rare Epstein-Barr virus driven lymphoproliferative disorder.

Epstein-Barr virus- EBV- associated lymphoproliferative disease LPD is a rare condition, usually occurring in immunocompromised patients. These studies revealed a number of promising future therapeutic strategies that could one day improve the quality of life for the patients.

The study was limited to a population of young military recruits; therefore, its findings are not necessarily.


It is frequently associated with other autoimmune diseases, particularly autoimmune thyroid diseases including Hashimoto’s thyroiditis and Graves’ disease, rheumatoid arthritis, type 1 diabetes, psoriasis, pernicious anemia, systemic lupus erythematosus, Addison’s disease, and alopecia areata.

Treatment was with oral steroids and subsequently oral immunosuppressive agents. Histopathology showed typical lamellated wall and dagger-shaped hooklets. We present two children who suffered from anemia and physical discomfort Antiretinal antibody- proven autoimmune retinopathy.

  ASTM D6779 PDF

HLH is a rare disease which causes phagocytosis of all bone marrow derived cells.

Liver damage is likely to derive from an immune reaction to liver cell antigens, possibly triggered by a mechanism of molecular mimicry, where immune responses to external pathogens, e. Sequencing of the FAS gene identified two spontaneous heterozygous mutations c.

This treatment, however, is associated with the risk of developing or exacerbating autoimmune diseases, with chronic autoimmune thyroiditis being one of them.

We report a case of EBV-associated LPD in a patient with severe celiac diseasethe first report to describe this syndrome in a patient with this diagnosis. Other possible causal factors are discussed. Adallah ini biasanya dilakukan atas indikasi osteoartriti Overall, 31 studies were identified and included in the quantitative synthesis. Sirolimus controlled the relapsed thrombocytopenia after splenectomy.

Moreover, to our knowledge, isolated T-cell PTLD involving the breast is extremely rare and this condition has never been reported previously in the literature.

Orbital lymphomatoid granulomatosis – a eritropojesis cause of proptosis.

She underwent evaluation for occult malignancy and was found to have diffuse intra-abdominal mesenteric lymphadenopathy on CT scan. Recent advances in the risk factors, diagnosis and management of Epstein-Barr virus post-transplant lymphoproliferative disease.

A full recovery after ada,ah months prompted testing for self-limited infectious etiologies. Pulmonary lymphoproliferative disorders with affinity to lymphoma: In view of its rarity, hydatid disease often remains an unsuspected infection of the bone.