תוצאת חיפוש

שרון אהרוני(1), יהודה נופך מוזס(2), אבינועם רחמל(1), מיכאל שוורץ(2), שי אשכנזי(1,3)

(1) המח' לרפואת ילדים א', (2) המח' לדימות ילדים, (3) היח' למחלות זיהומיות בילדים, מרכז שניידר לרפואת ילדים בישראל, פתח תקווה, והפקולטה לרפואה סאקלר, אוניברסיטת תל-אביב

סטרפטוקוק ביתא-המוליטי מקבוצה A (סבה"א) רגיש בכל העולם לפניצילין. אף-על-פי-כן, חלק מהזיהומים הנגרמים מחיידק זה הם קשים וממושכים, ולעתים הם אף קטלניים.

במאמר זה מובאת פרשת חולה – ילד עם דלקת-ריאות מורכבת המלווה בתפליט צידרי, שהחלים באופן איטי ולאחר טיפול ממושך. המטרה בהבאת פרשת-חולה זה היא להדגיש את החומרה, הסיבוכים והמהלך הממושך של דלקת-ריאות עקב סבה"א בילדים. אבחנה נכונה חיונית לשם מתן טיפול מתאים של פניצילין לתוך-הווריד לתקופה ממושכת.

רוני שילה (1), דורית יודשקין-פורת (2), אבי ויצמן (1,2),

(1) מח' א', (2) מח' ה', (1,2) המרכז לבריאות הנפש גהה

קלוזפין הוא תרופה ממשפחת הדיבנזודיאזפינים, הנמנית עם קבוצת התרופות נוגדות הפסיכוזה שאינן טיפוסיות (atypical antipsychotics). ייחודו העיקרי של קלוזפין הוא בהיותו בעל יעילות קלינית טובה יותר בדיכוי תסמינים פסיכוטיים בקרב חולים סכיזופרניים העמידים לטיפול בתרופות נוגדות-פסיכוזה טיפוסיות וביכולתו לשפר, בנוסף לתסמינים חיוביים, גם תסמינים שליליים בחולים אלה. יתרון התרופה הוא בהיותה בעלת מיעוט השפעות לוואי חוץ פירמידיות או מסכנות חיים, כדוגמת תיסמונת נירולפטית ממאירה [neuroleptic malignant syndrome (NMS)]. קלוזפין מאופיין, בניגוד לתרופות נוגדות-פסיכוזה טיפוסיות, בדיקה חלשה יחסית לקולטנים דופאמינרגיים קליפתיים מסוג D₂ לעומת D₄ ובפעילות חוסמת (blocker) חזקה בקולטנים סרוטונרגיים מסוג 5-HT₂. כמו-כן, לקלוזפין פעילות חוסמת חזקה בקולטנים אדרנרגיים מסוג אלפא-1 ואלפא-2, כולינרגיים, מוסקריניים והיסטאמינרגיים מסוג H₁.

Eosinophilic Ascites - Presenting Symptom of the Hypereosinophilic Syndrome

Sofia Rimbrot1, Michael Bennett², Marina Komorovski², Yishai Levy³

¹Department of Medicine A, ²Department of Haematology, Haemek Medical Center, Afula and ³Technion Faculty of Medicine, Haifa, Israel

We report a case of a 22 year old man with a history of bronchial asthma, suffering from diarrhea, eosinophilic ascites and prominent blood and bone marrow eosinophilia. The patient responded to corticosteroid treatment.

Later, hydroxyurea was added to this treatment because of recurrence of eosinophilia, ascites and hepatosplenomegaly.

Eosinophilic ascites is rarely the outstanding symptom of the hypereosinophilic syndrome.

Following the exclusion of other reasons for eosinophilia, concomitant unexplained hepatosplenomegaly suggested the diagnosis of a hyperereosinophilic syndrome.

אדם מור ויוסף מקורי

המחלקה לרפואה פנימית ב', בית-חולים מאיר, כפר סבא

תיסמונת יתר-אאוזינופילית ראשונית (תי"א), היא מצב המאופיין ביצירה קבועה ומוגברת של אאוזינופילים. לקביעת אבחנה זו צריכים להתקיים שלושה תנאים: מספר אאוזינופילים בדם ההיקפי הגדול מ-1,500 תאים לממ"ק למשך תקופה של שישה חודשים לפחות, העדר אטיולוגיה אחרת המסבירה את האאוזינופיליה וכן סימנים ותסמינים המעידים על מעורבות איברים מישנית לאואזינופיליה. ההסתמנות הקלינית של תי"א מגוונת ביותר. הביטוי הראשון יכול להיות פתאומי כתוצאה ממעורבות הלב ומערכת העצבים, או הדרגתי וכללי: עייפות, שיעול, קוצר-נשימה, כאבי-שרירים, חום והזעות. המספר הממוצע של כלל הליקוציטים נע בין 9,000 ל-25,000 תאים לממ"ק, כאשר מתוכם כ-30% עד 70% הם אאוזינופילים.

Eosinophilic Pneumonia induced by Minocycline

Eli Rosen

Medical Dept. B, Hillel Yaffe Hospital, Hadera

Eosinophilic pneumonia is a rare adverse effect of minocycline. To date there are about 70 chemical compounds that cause drug-induced, eosinophilic lung disease.

A 20-year-old woman who developed eosinophilic pneumonia due to minocycline is described. Diagnosis was established by history, signs and symptoms, peripheral eosinophilia, chest x-rays and response to combined cessation of treatment and a short course of steroids.

Physicians should be aware to this rare adverse effect of the drug. Attention to the possibility of minocycline-induced eosinophilic pneumonia can prevent unnecessary, expensive investigation. Cessation of intake is usually sufficient for cure.

Minocycline Pneumonitis and Eosinophilia

Noam Fink, Meir Mouallem

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

Pneumonitis with eosinophilia is one of the less common and severe adverse effects of minocycline. The disease evolves in days or weeks from the beginning of treatment, and is usually characterized by dyspnea, fever and bilateral infiltrates in the chest X-ray. With cessation of the antibiotic, and sometimes adding cortico-steroids, clinical and roentgenological resolution follow.

We present a case given minocycline for folliculitis and 3 weeks later fever, cough and shortness of breath developed. The clinical and roentgenological course was consistent with minocycline pneumonitis accompanied by eosinophilia.

Follicular Splenic Lymphoid Hyperplasia Associated with EBV Infection

Boleslaw Knobel, Enrique Melamud, Sharon Nofech-Moses, Liliana Zeidel

Dept. of Medicine B and Institute of Pathology, Edith Wolfson Medical Center, Holon and Sackler Faculty of Medicine, Tel Aviv University

Massive splenomegaly is defined as a spleen weighing about 10 times normal weight. We describe a 36-year-old man who had huge splenomegaly and secondary pancytopenia simulating malignant lymphoma for about 3 months. Splenectomy was necessary because of the suspicion of hematologic malignancy, especially isolated lymphoma of the spleen, and pain and mechanical abdominal disturbances.

On operation, the spleen was 25 cm long and weighed 250 g. There was florid, reactive follicular lymphoid hyperplasia. Immunohistochemical staining with CD-20(L26), CD-45Ro(UCHL), bcl-2 oncoprotein (Dakopatts), EBV (anti-EBV mol weight 60 KD, Dakopatts) was consistent with reaction to EBV infection and not with follicular lymphoma. Lack of PCR amplification using DNA extracted from paraffin-embedded splenic tissue indicated absence of a monoclonal B cell population carrying rearranged immunoglobulin genes. The lymphocytic population was proven polyclonal by the negative results of PCR for the bcl-2 gene rearrangement. EBV seroconversion from high titer antibodies of anti-EBV-VCA-IgM to negative, and from negative EBNA to positive was consistent with an apparent primary EBV infection.

We have not found on computerized search a previous report of reactive follicular splenic hyperplasia to EBV infection causing huge splenomegaly, with or without EBV-induced infectious mononucleosis.

Legionellosis in Israel

Ida Boldur, Silviu Hoffmann, Regina Kazak, Batzion Benjamin

Institute of Microbiology, Assaf HaRofeh Medical Center, Zrifin and Dept. of Life Sciences, Bar-Ilan University, Ramat Gan

Infection with Legionella remains an important cause of disease and death. We analyzed our laboratory data from 1993 through 1997, augmented by our 20 years of experience. The incidence of Legionella as a cause of pneumonia varied in our study from 5%-9%, with a slight increase during the winter. Isolation of these microorganisms from different water sources was higher during the summer and ranged from 7%-70%.

Special laboratory tests are necessary to diagnose the disease and monitor these bacteria in water samples. The serologic method - indirect immunofluorescent assay -- for 41 serogroups of Legionella was the main diagnostic method used. Legionella sg. 1 was the most frequent cause of the disease, with an incidence of 52% in 1993, decreasing to 15% in 1997. An increase in the incidence of seropositivity to "other Legionellae" is characteristic for our country.

No correlation was found between the incidence of isolation of a specific strain and exposure. However, it is well known that the disease is overtreated but underdiagnosed, which requires reversal. Larger studies of Legionella colonization in water supplies and in air are needed in order to establish the risk of infection. Water sources are presently under-studied, as are respiratory devices in hospitals, or they are not studied at all in Israel, such as in mist machines in supermarkets, in dental clinics, and in ships and airplanes.

The Mitrofanoff Pouch in Lower Urinary Tract Reconstruction

J.H. Pinthus, Y. Mor, J. Ramon

Urology Dept., Chaim Sheba Medical Center, Tel Hashomer

The Mitrofanoff principle, first described in 1980, consists of implanting a tubular organ such as the appendix, ureter, or fallopian tube into the wall of the bladder (or urinary reservoir) to create a non-refluxing, catherizable urinary conduit. Between 1993-1996, 7 men and 1 woman (aged 48-64, average 59) underwent radical cystectomy and urethrectomy combined with the creation of a MAINZ I urinary reservoir (based on the Mitrofanoff principle). In men the indication for the procedure was the diagnosis of invasive transitional cell carcinoma of the bladder with involvement of the prostatic urethra. All patients had refused urinary diversion to an ileal conduit because of its deleterious effect on the quality of life.

In all patients the postoperative course was uneventful, apart from intraperitoneal urinary leakage from the reservoir in 1, successfully managed conservatively. The patients have gained full control of urinary drainage, performing intermittent self-catheterizations every 4-5 hours. In 3 patients there were difficulties with catheterization due to stenosis of the conduit, usually at the skin level. None have suffered leakage from the reservoir, during the day, even when it was full.

Our experience shows that creation of a continent urinary reservoir according to the MAINZ I technique is an excellent surgical solution for patients in whom the creation of an orthotopic reservoir is impractical. The use of the umbilicus as a stomal site preserves normal body image and thus does not interfere with quality of life as in those undergoing radical cystectomy.

Kimura's Disease and Angio- Lymphoid Hyperplasia

Henia Lichter, Karol Segal, Celia Mor, Raphael Feinmesser

Depts. of Ophthalmology, Otolaryngology and Pathology, Rabin Medical Center (Beilinson Campus), Petah Tikva, and Sackler Faculty of Medicine, Tel Aviv University

Kimura's disease is a rare angiolymphoid proliferative disorder of soft tissue characterized by subcutaneous swelling and a predilection for the head and neck. There are usually enlarged regional lymph nodes, eosinophilia and elevated sedimentation rate and IgE levels. A 26-year-old women with subcutaneous masses in the submandibular area is reported. The diagnosis of Kimura's disease versus angiolymphoid hyperplasia is discussed.

Progression of Diabetic Retinopathy after Cataract Extraction

Y. Raniel, Y. Teichner, Z. Friedman

Annette and Aron Rozin Dept. of Ophthalmology, Bnai-Zion Medical Center and Bruce Rappaport Faculty of Medicine, The Technion, Haifa

A prospective study of the effect of cataract extraction with intraocular lens implantation on the course of diabetic retinopathy (DR) in 44 patients (59 eyes) was carried out. It showed that in the 1-3 years following surgery, there was progression of DR (including development of newly formed retinopathy) in 35% of the patients (28.8% of eyes). Progression was more marked in patients with pre-operative bilateral DR compared to those without bilateral DR (77% and 16% respectively). Insulin dependence did not play a role in progression. Final visual acuity was better in patients without pre-operative DR, as well as in eyes without progressive retinopathy.

Central Cord Syndrome in the Elderly Who Fall: a Diagnostic Trap

A. Adunsky, H. Semo, S. Levenkrohn

Geriatric Rehabilitation Dept., Chaim Sheba Medical Center, Tel Hashomer

Acute post-traumatic spinal injury is common and usually poses no diagnostic difficulties. Following a low-energy fall, the onset of acute central cord syndrome in the elderly is not common and is frequently misdiagnosed. Men aged 60 and 81, and a woman aged 75 are described, in whom central cord syndrome was overlooked. Awareness of this condition is important to avoid incorrect diagnosis and hazardous management.

Temporal Hemianopia And Diabetes Insipidus Following Head Injury

M. Zaaroor, D. Goldsher, M. Feinsod

Center for Treatment and Applied Research in Head Injuries, Dept. of Neurosurgery and Diagnostic Radiology Dept., Rambam Medical Center and Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa

Bitemporal hemianopia and diabetes insipidus following head injury are caused by a lesion in the center of the optic chiasm, together with injury to the adjacent pituitary stalk or the hypothalamus. This combination was thought to be a rare complication of severe head injury. The case of a 16-year-old male is presented, which together with recent reports suggests that this relatively under-recognized syndrome is not infrequent, that it may follow even minor head injury, and that magnetic resonance imaging can demonstrate the chiasmal lesion.