عنوان
: نارسائي
حادكليه
دربيماران
مبتلا به ميلوم
مولتيپل و
گزارش چهار
مورد .
نويسندگان
: دكتر مجيد
مرتضوي ، دكتر
جليل واعظ
قراملكي ،
دكتر جمال
عيوضي ، دكتر
اشرف فخرجو
مقدمه
:
بدخيمي
هاي اعضاء
مختلف بدن
انسان عوارض
متعددي بر روي
كليه ها دارند
.
ميلوم
مولتيپل جزو
بدخيمي هاي
پلاسما سل است
. كه 1% كل بدخيمي
هاي بدن انسان
را تشكيل داده
ولي با 20%
نارسائي حاد
كليه ها همراه
است . افزايش توليد
بيش از حد
مقدار طبيعي
زنجيره سبك در
ميليوم مولتيپل
به علت كاهش Endocytosis
در توبول
ابتدائي كه با
ماكانيسمهائيكه
Receptor - mediated اند مي
تواند دفع بيش
از حد طبيعي
زنجيره سبك
پروتئينها
شود . ايجا د
نارسائي حاد
كليه هايكي به
علت توكسيك
بودن پروتئين
هاي زنجيره
سبك با مايع
توبولي به
توبولهابي
انتهائي
رسيده و در
اين قسمت از
توبول با
پروتئين Tamm-Horsfall تشكيل
سيلندر
تولبولي مي
دهد كه به وسيله
سلولهاي بزرگ
و داراي چند
هسته احاطه مي
شوند .
فاكتورهاي
كمك كننده
ديگري هم در
ايجاد نارسائي
حاد كليه وجود
دارند .
روش
:
تعداد 7
مورد بيمار
مبتلا به ميلوم
مولتيپل و
نارسائي حاد
كليه ها به
بخش همودياليز
بيمارستان
امام خميني (
ره ) معرفي شده
بودند و تحت
بررسي قرار
گرفتند .
نتايج
:
دو
مورد از
بيماران مونث
و 5 مورد مذكر
بودند . سن
آنها حداقل 33 و
حداكثر 73 سال
داشتند . در
تمامي موارد
دردهاي
استخواني ،
تهوع و استفراغ
شكايت اصلي
بودند .
كراتينين
خون بيماران
بين 14 – 5/7
ميلي گرم
درصد .
هموگلوبين
بين 2/9 - 2/5 گرم
درصد .
پروتئين Bence Jones ادراري
در تمامي
موارد مثبت
بوده و در الكتروفورز
پروتئينهاي
خون M – Band
ترسيم شده است
.
ESR
حداقل 70/30 و
حداكثر 172/160
ميليمتر
بودند .
اسيداوريك
خون بيماران
بين 8/7 - 5/10
ميليگرم
درصد بودند
كلسيم خون
بيماران در حد
طبيعي بودند .
بيوپسي كليه
فقط در يك
مورد از
بيماران به
عمل آمد ، كه
مويد كست
نفروپاتي بود
. آسپيراسييون
مغز استخوان در
تمام بيماران
به عمل آمده
ميلوم مولتيپل
را تشخيص
دادند .
ضايعات ليتيك
استخواني در
چهار موردبه
ثبت رسيده است
تمامي
بيماران تحت
درمان
سيتوتوكسيك و
همودياليز
قرار گرفتند .
يك بيمار بعد
از يكسال و دو
بيماربعد از
يك ونيم سال
فوت نمودند و
بقيه بيماران
تحت درمان مي
باشند .
نتبجه
گيري :
ازمرور
مقالات
منتشره و
بيماران
معرفي شده بر
مي آيد كه اولا
در بيماران با
دردهاي
استخواني و سن
بالاي 33 سال به
ميلوم
مولتيپل فكر
كرده و
اقدامات تشخيص
به عمل آيد .
ثانيا سعي شود
از عوامل تشديد
كننده
نارسائي حاد
كليه ها كه
بعدا ارائه خواهندشد
اجتناب گردد .
Title of Article : Acute renal failure in patients with
multiple myeloma and report of four cases
Author(s) : M.Mortazavi M.D, G.Vaezi-Garamalik M.D,
J.Eivazi M.D. , A.Fakhreju M.D .
Back ground and Aims :
To evlut the effect of Multiple myeloma on renal function .
Introcuction :
Malignacies of different organs of human body have several
complication on kidneys . Multiple myeloma (MM) is a plasma cell malignancy
which consist 1% of all human being malignancies , and is associated with 20%
of acute renal failure . Excess ptoduction of ligt chains in MM with reduction
in endocytosis in proxinmal tubule with receptor mediated mechanisms can lead
to loss of excess amounts of light chain proteins . Acute renal failure is due
to toxicity of light chain proteins in proximal tubules and damage of them . On
the other hands light chains reach with tubular fluid to distal tubules and
with Tamm-Horsfall protein forms tubular cylinders . This cylinders have large
and multinuclear cells . Other predisposing factors are on acute renal failure
.
Method :
Seven patients with MM and ARFwere refered to Imam
Khomeini hemodialysis ward and studied .
Results:
Two patient vere female and five male . Age was at least
33 and at least 73 . In al cases bone pains , nausia and vomiting were chief
compliant . Serum creatinie was between 7.5 and 14 . Hemglobin was 5.2-9 mg% .
Urinary Bence Jones protein was positive in all cases and in electrophoresis
M-Band was curved . ESR was at least 30/10 and at last 160/172 mm . Serum uric
acid was 7.8-10.5 . Serum calcum was in normal limi. Only one of patient was
biopsied which show cast nephropathy . Bone marrow aspiration was down in all
patients and MM was documented . Bone lysis was seen in 4 cases . All patients
were on cytotoxic tirapy and hemodialysis . One patien after one year and two
patient after 1.5 year died , and other . patient are under thrapy .
Conclusion :
Reviev of published arthicles and introduced patients
reveals that , in patients with bone pain and age over 33 years we must think
to MM and diagnostic procedures must be done , and predisposing factors for ARF
ought to be eliminated .
Title : IHOP protocol in refratory ALL
Author(s) : Eivazi J,MD. Nikanfar A,MD.
Adressf :
Tel : 3343811-13
E-mail: jziaei@hotmail.com
Introduction & Objective :
Acute lymphoblastic leukemia is biologically &
clinically a heterogenous group of diseases characterized by a malignant
proliferation of immature lymphoid cells in the bone marrow . Treatment of the
newly diagnosed patient with ALL,comprises four phases ; remission induction ,
CNS prophylaxis , postremisson consolidation and maintenance . Adult with
primary refractory or relapsed ALL have poor prognosis with current salvage
chemotherapies .
Methods :
To achieve complete remissions and prolonge remission
duration and long-term survival , we designed a combined salvage regimen IHOP
in 13 patients with refractory ALL. They treated with Ifosfamide 1 g/m2
on 1-5 day , Adriamycine 70 mg/m2 on day 1 , Vincristine 2 mg on day
1 , prednisolon 100 mg on day 1-5 .
Results :
Among 13 patients , 8 patients had treated with VP16
10 mg/kg on 1-3 day & CTX 50 mg/kg on day 1-2 , and 5 patients had treated
with standard regimen of ALL (v,p,c) . The severity of pancytopenia with IHOP
was less than VP16 & CTX , none of the patient had fever . One
of the patient who had treated with VP16 & CTX had complete
remission another patients had not response . After 6 month follow-up only two
patient alived and they treated with prednisolon & vincristine monthly .
One of the patients who treated with standard protocol of ALL had partial
remission , he treated with VP16 & CTX . After 6 month follow-up
all of the patient died except the patient who described above . This result
indicate that IHOP is not a promosing
therapy for treatment of refractory ALL .