תוצאת חיפוש

ראיד סלים, זהר נחום, אליעזר שלו

המח' לרפואת נשים ויולדות, מרכז רפואי העמק, עפולה והפקולטה לרפואה הטכניון - חיפה

תרומבוציטופניה (ת"ר) מוגדרת כמספר טסיות דם מתחת ל-150,000 למיקרוליטר, ושכיחה ב-7%-5% מההריונות, 75% מכלל מצבי ת"ר בהריון, הם תוצאה של תרומבוציטופניה הריונית (ת"ה), ב-20%-25% מהחולות ת"ר היא חלק מתיסמונת HELLP (hemolysis, elevated liver enzymes, low platelets) בנשים עם רעלת הריון. ארגמנת תרומבוציטופנית חיסונית (את"ח) מהווה פחות מ-4% מסך אירועי ת"ר בהריון. אבחנה מדויקת חשובה לשם מתן טיפול הולם מחד גיסא, ולשם מניעת פעולות מיותרות ומסוכנות, מאידך גיסא.

Malignant Humoral Hypercalcemia Associated with Angiotropic Large B Cell Lymphoma: Case Report

Boleslaw Knobel, MD;^1,5 Ilan Sommer, MD;¹ Pauline Petchenko, MD;² Dorit Lev, MD; ³ Elimelech Okon, MD;^4,5

¹Department of Medicine "B", ²Department of Hematology, ³Institute of Genetics, Edith Wolfson Medical Center, Holon ⁴Department of Pathology, Rabin Medical Center, Petach Tikva and 5Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

Angiotropic large B cell lymphoma (angiotropic LCL) or intravascular large cell lymphoma (IVLCL) was diagnosed by liver and bone marrow biopsies and immunohistochemical studies in a 52 year old Caucasian male.

IVLCL is a very rare disease characterized by widespread intravascular proliferation of lymphoma cells. Although it most commonly affects the central nervous system or skin and occasionally bone marrow, angiotropic LCL may be present without evidence of localized disease, as seen initially in our patient.

To date, only a few cases of intravascular malignant lymphomatosis associated with parathyroid hormone related protein (PTH-rP) induced humoral hypercalcemia have been published.

Our extraordinary case was diagnosed mainly by liver biopsy. The neoplastic lymphoid cells stained diffusely and strongly positive with CD-20 (Pan B) and were negative for CD-3 (Pan T) immunostain.

The most significant, initial clinical finding was severe, unexplained hypercalcemia (until 18.6 mg/dl). Plasma PTH-rP showed a ten-fold increase at 8 pmol/L (normal value less than 0.8 pmol/L). Very unusual cytogenic abnormalities were found.

The patient received the massive third generation combination chemotherapy comprising of Methotrexate, Doxorubicine, Cyclophosphamide, Vincristine, Prednisone and Bleomycin and developed, complete although temporary, clinical, humoral and cytogenetic remission.

Interactive Health Databases on the Internet

Fabienne Sikron, Vita Barell

Health Services Research Unit, Ministry of Health

In order to obtain reliable, comprehensive and current data, information systems which enable flexible presentation or analysis are necessary, as opposed to static tables. On-line and interactive numeric health databases on the Internet are increasingly available. Interactive tables can be produced in many fields, eg., mortality, hospitalizations, cancer incidence, or motor vehicle accidents. The query screens are user-friendly and they can access remote, computerized data. Thus, it is possible to receive immediate responses to specific questions from national or international datasets, which can then be compared with local data - all without leaving one's chair. The aim of this review is to increase awareness of the existence of numeric health databases on the Internet, and their contribution to epidemiological research.

בן-עמי סלע

המכון לכימיה פתולוגית, מרכז רפואי שיבא, תל-השומר; החוג לביוכימיה קלינית, הפקולטה לרפואה סאקלר, אוניברסיטת תל-אביב

החשיבות של יציבות המירקם החוץ-תאי (extracellular matrix, להלן EMC) בשמירת שלמות דופן כלי הדם מוכרת היטב, בין השאר מהבנת מחלות בהן נפגעת שלמות EMC, כמו לדוגמה בתיסמונת Marfan. כשמעלים את נושא ה- EMC, מוזכרת בנשימה אחת קבוצת אנזימי המירקם נושאי האבץ, MMP, בשל חשיבות פעולתם הפרוטאוליטית בפירוק של רוב המרכיבים החלבוניים במירקם האמור. על חשיבותם האבולוציונית של אנזימי MMP תעיד העובדה, שעד היום זוהו 66 אנזימים כאלה החל ביצורים ירודים כמתגים מסוימים, ועד לאדם, בו התגלו עד כה 21 אנזימים ממשפחה זו. במקביל נתגלו  4 חלבוני ריקמה (tissue inhibitors of MMP, או TIMP), היוצרים קשר לא-קוולנטי עם האנזימים האמורים ומנטרלים את פעולתם. אנזימי MMP מופרשים כזימוגנים בלתי-פעילים אנזימית, ושיפעולם נעשה באמצעות פרוטאינאזות אחרות כפלסמין, טריפסין ולפחות MMP ממברנתי אחד שכינויו –MT-MMP, המבקעים פפטיד קצר בזימוגן, ומביאים להתמרתו ל- MMP פעיל. בסקירה קודמת בעיתון זה, ייחדנו מקום לחשיבותם של אנזימי המירקם הללו בתהליך הסרטני, ואילו בסקירה הנוכחית יורחב הדיון למשמעויות של אנזימי MMP בהיבטים אחדים של כלי הדם.
 

Metallic Stents for Acute Colonic Obstruction

M. Itkin, E. Atar, H. Neuman, D. Kravarosic, Z. Fuko, M. Kaz

Radiology and General Surgery B Depts., Golda Campus; and General Surgery Dept., Beilinson Campus; Rabin Medical Center, Petah Tikva

The traditional treatment of acute colonic obstruction, usually caused by malignant tumor, is a 2-stage surgical procedure. The first operation is emergent and includes primary tumor resection and end colostomy followed by scheduled colostomy closure. These operations are associated with high mortality and morbidity. Recently, insertion of self-expanding metallic stents for temporary colonic decompression has been was introduced. With this new technique colostomy can be avoided in the acute phase.

In advanced colonic cancer stent-insertion is the only palliative treatment. It is done in the radiology department under fluoroscopic guidance. We present 2 cases of malignant colonic obstruction treated successfully by stent insertion.

Intraventricular Hemorrhage in Full-Term Neonates

S. Menascu, A. Levitas, A. Golan

Pediatrics B Dept., and Newborn and Preterm Dept., Soroka Medical Center and Ben-Gurion University of the Negev, Beer Sheba

Intraventricular hemorrhage in full-term neonates is rare; it may develop without any clinical signs. Its cause is not fully understood although some risk factors have been identified. A higher index of suspicion would ensure earlier diagnosis and treatment, which might reduce the rate of severe complications. We describe 2 cases in full-term neonates.

ענבר צוקר¹, לאה סירוטה¹, נחמה לינדר¹

¹המח' לטיפול נמרץ פגים, מרכז שניידר לרפואת ילדים בישראל, פתח-תקווה

ילודים, ובמיוחד פגים במשקל לידה נמוך, נמנים עם קבוצות החולים הנזקקות בשכיחות גבוהה לערויי-דם ותוצריו. על פי הערכות, כ- 80% מהילודים השוקלים פחות מ- 1500 ג', יקבלו מספר ערויי-דם בשבועות הראשונים לחייהם. ערויים אלה ניתנים כדי לתקן אנמיה תסמינית, הנגרמת כתוצאה ממישלב של חסר ייצור מספיק של דם ע"י הילוד ובמיוחד הפג הגדל, ושל איבודי דם מישניים לבדיקות. לעיתים, ניתנים ערויים במסגרת פעולות טיפוליות מיוחדות, המצריכות מתן ערויי דם בכמות גדולה, כגון ניתוחי לב וערוי חלופין. הטיפול בערויי דם יכול לגרום לשורה של סיבוכים מיידיים ומאוחרים. חלקם יכולים לחול בכל קבוצת גיל וחלקם ייחודיים לילודים. המטרה בסקירה זו היא לדווח על הסיבוכים האפשריים של ממתן ערוי-דם בילודים, תוך התייחסות למאפיינים הייחודיים לתת-אוכלוסייה זו של חולים.
 

Retinal Injury Induced by Laser Pointers

D. Israeli, Y. Hod, O. Geyer

Eye Dept., Carmel Medical Center, Haifa

Laser pointers originally designed for use during presentations are ubiquitous and are even sold as toys (such as pens or on key chains) in drug stores. Though reported as safe, the laser pointers still carry the risk of potential damage to the eye. We report a 16-year-old boy with bilateral retinal injury caused by 20-30 seconds of exposure to a laser pointing-device. Immediately thereafter, vision was blurred bilaterally and he noted a central red scotoma in each eye. Symptoms resolved spontaneously within 2 days but the retinal scars remained all during the 10 months of follow-up.

It is clear from our report and 3 other publications that retinal damage can develop from misusing laser pointers. Laser hazards and safety should be stressed for the general public. We recommend that laser-pointers should not be available as toys to children and teenagers.

Prevention and Treatment of Procedural Pain in Pediatric Wards

R. Gorodischer, L. Herzog, E. Herzog

Depts. of Pediatrics A and Anesthesiology, Soroka University Medical Center; and Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer Sheba

Present knowledge and available pharmacological agents allow for adequate prevention and treatment of pain in children. We present guidelines we prepared for the prevention and treatment of procedural pain in children in our general pediatric ward. This followed extensive review of the literature, participation in scientific meetings, discussions with experts and consultation with interested clinicians. Successful implementation of the guidelines requires increased appreciation of the importance of pain prevention, participation of the nursing, as well as medical staff, and ability to evaluate pain in children of various ages.
 

A Molecular Method of Diagnosis of Congenital Adrenal Hyperplasia

Shoshana Israel, Chaim Brautbar

Tissue Typing Unit, Hadassah Medical Center, Jerusalem

Congenital adrenal hyperplasia (CAH) is caused mainly by deficiency of the 21-hydroxylase enzyme. The disease may appear in the classical salt-losing, simple virilizing forms or as a mild, nonclassical form. 21-hydroxylase is encoded by the CYP21B gene on the short arm of chromosome 6, in the midst of the human leukocyte antigen (HLA) complex, between HLA Class I and Class II regions.

We describe a method for identifying mutations in the CYP21B gene. It is based on amplification of the gene using the polymerase chain reaction and identification of mutations with sequence-specific oligo-probes. The mutations identified were: V281 and P30L responsible for nonclassical CAH, and I2 splice, Q318X, I172N, cluster E6, and a deletion including 8bP in the third exon (8bP del) responsible for the classical form of CAH.

We also analyzed 2 families affected with the classical form of CAH which demonstrate possible complications in genotyping. Typing for HLA haplotypes can be helpful in certain cases, as demonstrated in 1 of the families presented. In this case it was necessary to distinguish between 2 possible genotypes: 1 with the mutations in tandem on 1 chromosome and the other with the mutated genes on both chromosomes. HLA haplotyping enabled the assignment of the mutations to the relevant chromosomes and thus allowed correct genetic counseling.

The other family demonstrated the importance of CYP21B genotyping in individuals with the nonclassical form of CAH. This form may consist of 1 mild and 1 severe mutation, representing a serious potential for transmitting the classical form of CAH.

Atrophic Gastritis Presenting with Pulmonary Embolism

Muhammad A. Abdul-Ghani, Rima Feldman, Moshe Shai, Jacob Varkel

Dept. of Medicine C, Western Galilee Hospital, Naharia

Atrophic gastritis is an autoimmune gastropathy in which there is destruction of gastric parietal cells. This results in intrinsic factor deficiency and disturbance in vitamin B12 absorption. Its clinical manifestationa are therefore the consequences of B12 deficiency and include anemia and neurological defect. In addition, lack of B12 results in metabolic changes, including disturbances of methionine metabolism and accumulation of homocysteine.

In recent years, there has been increasing evidence suggesting that hyperhomocysteinemia is a risk factor for thrombo-embolic disease. We describe a 51-year-old man with atrophic gastritis, severe B12 deficiency and hyperhomocystein-emia. The initial clinical manifestation was pulmonary embolism, without either anemia or neurological signs. B12 deficiency should therefore be considered in patients being investigated for hypercoagulability.

Pulmonary Adenocarcinoma in Myasthenia Gravis - Auto-Immunity and Late Development of Malignancy

Yitzhak Rosen, Yair Levy, Yehuda Shoenfeld

Dept. of Internal Medicine B, Sheba Medical Center, Tel Hashomer and Sackler Faculty of Medicine, Tel Aviv University

We report a 75-year-old man with myasthenia gravis for many years, who was hospitalized because of cough, fever, and dyspnea. Chest x-ray revealed a bilateral pleural effusion. Adenocarcinomatous cells were found in the pleural fluid. Computerized tomography of the chest showed widespread pulmonary dissemination of the tumor.

The relationship between myasthenia gravis, an autoimmune disease involving the motor end-plate, and malignancy (thymoma) has been widely recognized. Current literature documents few reports of lung malignancies with concurrent development of myasthenia gravis. A tentative explanation, based on current research, is provided for the possible role of myasthenia gravis and the late development of lung cancer. Moreover, a model for the autoimmune phenomenon and the development of late malignancies will be provided with explicit explanations. It is important to search for occult, developing malignancies in newly diagnosed autoimmune diseases.

Coloring the Floor of Schlemm's Canal in Deep Sclerectomy

Ben Zion Silverstone

Eye Dept., Shaare Zedek Medical Center, Jerusalem

Increased intraocular pressure in glaucoma, resistant to maximal tolerated medical therapy, can be relieved by deep sclerectomy. Its advantage over classical trabeculotomy is fewer postoperative complications. This probably results from its being relatively noninvasive, since the anterior chamber is not penetrated.

Successful deep sclerectomy requires preservation of the trabeculo-descemetic membrane, which forms part of the floor of Schlemm's canal. Aqueous flows from the anterior chamber across the trabeculo-descemetic membrane and into the ocular venous drainage. Despite the importances of its preservation, during deep sclerectomy it is perforated in 10-15% of cases.

Coloring the endothelium lining the floor of the canal with gentian violet solution improves visualization of the membrane and thus aids in its preservation. Its use makes the procedure easier and should improve results.

Gastrointestinal Hemorrhage of Obscure Origin

Yoel Siegel, David Ergaz, Oscar Liphshitz, Felix Gottesfeld, Zev Sthoeger

Depts. of Medicine B and Surgery, and Gastroenterology Unit, Kaplan Medical Center, Rehovot (Associated with Hebrew University-Hadassah Medical School, Jerusalem)

Gastrointestinal bleeding of obscure origin consists of recurrent bouts of acute or chronic bleeding for which no definite source is discovered in routine endoscopic and barium contrast studies of the upper and lower gastrointestinal tracts. Usually its cause is angiodysplasia of the intestine, but many cases are due to tumors, mostly of the small bowel, which may be malignant.

In patients under the age of 50, the proportion with malignancy is relatively high (up to 14%) as compared to older patients. We describe a 45-year-old woman who suffered from gastrointestinal bleeding for 3 years. The cause of bleeding was not found despite extensive work-up.

In her last admission for acute gastrointestinal hemorrhage she was given a total of 30 units of blood. A tumor of the small intestine found by angiography was excised and found to be a stromal tumor of uncertain malignant potential. 1 year after operation she is asymptomatic without bleeding and her hemoglobin is stable without treatment.

Hospitalization for Renal Colic: Epidemiological Features and Clinical Manifestations

Yahav Oron, Amir Shahar, Eran Dolev

Sheba Medical Center, Tel Hashomer; Israel Defense Forces Medical Center; Meir General Hospital, Sapir Medical Center, Kfar Saba; and Dept. of Medicine H, Sourasky-Tel Aviv Medical Center

The medical records of all patients referred to the emergency department (ED) of Sheba Medical Center for renal colic during 1996 were analyzed. Patients discharged from the ED and those hospitalized were compared.

There was no significant difference between the 2 groups with regard to average age or sex distribution. Statistically significant differences were found with regard to frequency of chills and fever, history of renal colic, referral for renal colic during that year or hospitalization for renal colic or nephrolithiasis, previous positive imaging, stone removal by surgery or extracorporeal shock wave lithotripsy, fever exceeding 37.5^o and administration of fluids, pethidine or pramin in the ED, prolonged stay in the ED and previous appendectomy.

A conditional regression model tested the predictive value of each of those factors. Inclusion of independent variables into the model led to an overall correct classification rate of 84.43%, with 44.83% sensitivity and 93.16% specificity. There were correlations between referrals for renal colic, overall renal colic rate and average monthly temperature, so there was no pure correlation between average monthly temperature and referrals to the ED for renal colic.

The major indications for hospitalization were actually the clinical ones, indicating either an active metabolic disease or suspected obstruction of the urinary tract. Treatment in the ED and duration of the visit indicated disease severity.