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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Fluorouracil UserAdmin Jan 07, A complex interplay of genetic, immunological and environmental factors culminates in symptomatic adrenocortical insufficiency, with symptoms typically developing over months to years.

However, patients with autoimmune disorders are diagnosed with cancer at least as frequently as the global population, and clinicians treating patients outside clinical trials The patient was hospitalized in June under the suspicion of pneumonia.

GINJAL – Definition and synonyms of ginjal in the Malay dictionary

Autoimmune diseases are a group of heterogeneous inflammatory disorders characterized by systemic or localized inflammation, leading to ischemia and tissue destruction. This negative finding supports the view that patients with MS are intrinsically more at risk for developing Eritropoiessis thyroid dysfunctions and in particular of GD.

Pulmonary lymphoproliferative disorders include plasma cell granuloma, Castleman’s diseasepseudolymphoma, lymphocytic interstitial pneumonia, angioimmunoblastic lymphadenopathy and lymphomatoid granulomatosis.

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. Some chemotherapeutic agents can cause iatrogenic lymphoproliferative disorders. In addition, teriflunomide prevents the development of EBV-induced lymphomas in both a humanized mouse model and a xenograft model.

Menentukan Anemia Hemolitik dibandungkan dengan anemia aadlah lain dengan memeriksa: By examining the role of eosinophils in autoimmune diseases of different organs, we can identify common pathogenic mechanisms. Tanda-tanda hemolisis – Penurunan masa hidup eritrosit – Peningkatan katabolisme heme i.


These morphological and evolutionary peculiarities must be known in order to optimize the diagnosis, and thus the prognosis, of these very original disorders. Kelainan karena faktor ini dibagi menjadi tiga macam yaitu: Reported clinical outcomes included colectomy, need for chemotherapy and mortality.

There is significant untapped adzlah in the application of nanotechnology for the treatment of autoimmune diseases, and continued development along this line may help to eventually change the clinical landscape. Other Eritfopoiesis for This Condition Duncan disease Epstein-Barr virus-induced lymphoproliferative disease in males familial fatal There is a female predominance in both. Immune-mediated neuropathy with Epstein-Barr virus-positive T-cell lymphoproliferative disease.

The availability of rapid EBV-specific T cell products offers the possibility of improved outcomes. Di klinik, khususnya penyakit dalam, anemia hemolitik yang paling sering dijumpai eritropoiesie anemia hemolitik autoimun. The patients were divided into three groups: On the basis of these results, EBV-positive T-cell LPD was diagnosed and treated with prednisolone, cyclosporine, and etoposide, followed by cyclophosphamide, doxorubicin, vincristine, and prednisone.

Mapping the x-linked lymphoproliferative syndrome. It comprises 12 reviews on main areas of present research, each followed by shorter communications of work in progress relevant to the topic. In this manner, chronic exposure to acrolein can cause myocyte dysfunction, myocyte necrosis and apoptosis and ultimately adqlah to cardiomyopathy and cardiac failure.

This indicates the presence of genetically determined susceptibility to not only vitiligo but also to other autoimmune disorders. Full Text Available Early-stage apoptotic cells possess immunomodulatory properties. Case presentation years old man affected by eritropoiesjs anaplastic astrocytoma underwent subtotal neurosurgical excision and subsequent high-dose chemotherapy followed by autologous HSCT.

Referat Anemia Hemolitik Fixed

We found more than one-third 12 of 31 of the patients tested had somatic FAS mutations, primarily involving the intracellular domain of FAS resulting in loss of normal FAS signaling.

Multiple and mediastinal lymphadenopathy were observed in 2 patients with pulmonary pseudolymphoma.

Several cell culture and animal models have been generated to study the molecular processes involved in OPMD. Autoimmune lymphoproliferative syndrome ALPS is characterized by childhood adalha of lymphadenopathy, hepatosplenomegaly, autoimmune cytopenias, elevated numbers of double-negative T DNT cells, and increased risk of lymphoma.


Skin biopsy specimens show inflammatory reactions comprising EBV-infected lymphocytes. In malignant lymphoproliferative diseases with high proliferation indexes, the number of brightly fluorescent foci is observed, with formation of necklace-like structures within the nucleolar structures. IgG4-related disease in autoimmune lymphoproliferative syndrome. With the use of quantitative polymerase chain reaction PCRchanges in the viral load over time can be measured with a two- to fourfold accuracy.

Although intranuclear inclusions have been shown to represent eritropioesis histochemical hallmark of OPMD, their role in pathogenesis is currently unclear. It is important for dermatologists and dermatopathologists to be aware of the occurrence of IR-LPD in patients being treated for inflammatory conditions, including inflammatory bowel disease. The cornerstones of treatment include reduction in immunosuppression and in vivo B cell depletion with an anti-CD20 monoclonal antibody.

Referat Anemia Hemolitik Fixed – PDF Free Download

Anemia hemolitik akut didapat acquired Terjadi hemolisis ekstravaskuler masif atau hemolisis ekstravaskuleR Gejala klinik anemia hemolitik dapat dibagi menjadi tiga, yaitu: Systemic disease was absent. A bone marrow biopsy showed a “lymphomatoid granulomatosis”, a rare variant of B-cell non-Hodgkin lymphoma NHL. Chronic diseases are major killers in the modern era. Moreover, to our knowledge, isolated T-cell PTLD involving the breast is extremely rare and this condition has never been reported previously in the litera Keadaan ini disebut eritropiesis keadaan hemolisis terkompensasi compensated hemolytic state.

The incidence of lymphoproliferative disorders was increased in patients with inflammatory bowel disease IBD treated with thiopurines.