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1.
Pediatr Surg Int ; 25(7): 617-21, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19479267

ABSTRACT

PURPOSE: Solid pseudo-papillary tumors (SPT) are rare pancreatic neoplasms of low-malignant potential occurring mainly in young women. The purpose of this report is to describe our experience with laparoscopic management of these tumors with 4-year follow-up. METHODS: Three children with SPT were admitted to two hospitals in Paris, France, between February 2000 and December 2006. Diagnosis or treatment was carried out using laparoscopic techniques (biopsy and resection in one case and biopsy only in two). Long-term follow-up data were collected. RESULTS: All three patients presented recurrences within 3 years after resection, i.e., disseminated peritoneal recurrence in two patients and local recurrence in one. The two patients with peritoneal recurrences were treated by surgical resection and chemotherapy. The patient with local recurrence could not be treated due to contraindicating local factors. All three patients were alive at the time of this writing. CONCLUSION: This is the first report describing long-term follow-up after laparoscopic management of SPT. All three patients developed recurrences. These poor results contrast sharply with the low risk of local or disseminated recurrence after open laparotomy without chemotherapy that has been considered as the treatment of choice up to now. Recurrences after laparoscopic management may have been due to diffusion of tumor cells caused by gas insufflation especially during biopsy. Laparoscopic biopsy should not be performed in patients presenting SPT.


Subject(s)
Cystadenoma, Papillary/diagnosis , Cystadenoma, Papillary/surgery , Laparoscopy/methods , Neoplasm Recurrence, Local/secondary , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/surgery , Peritoneal Neoplasms/secondary , Biopsy/methods , Child , Cystadenoma, Papillary/pathology , Female , Follow-Up Studies , Humans , Male , Minimally Invasive Surgical Procedures/methods , Pancreas/pathology , Pancreas/surgery , Pancreatic Neoplasms/pathology , Peritoneal Neoplasms/drug therapy , Peritoneal Neoplasms/surgery , Rare Diseases
2.
Eur J Pediatr Surg ; 17(5): 328-34, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17968789

ABSTRACT

PURPOSE: Whereas gastrointestinal symptoms such as vomiting, diarrhea and abdominal pain are common in children suffering from the so-called post-diarrheal form (D+) of hemolytic uremic syndrome (HUS), more serious gastrointestinal complications are rare. We tried to define factors predictive of the severity of gastrointestinal complications post D+ HUS. METHODS: We reviewed the files of all children admitted to our hospital for D+ HUS between 1988 and 2000. We retained those cases with gastrointestinal complications and analyzed the consequences of these complications on the evolution of the children's conditions. RESULTS: Sixty-five children with D+ HUS were admitted to our hospital during this period. Sixteen children developed gastrointestinal complications involving one or more digestive organs: necrosis of the colon or ileum, hemorrhagic colitis, pancreatitis, transient diabetes, hepatic cytolysis and cholestasis, peritonitis and prolapse of the rectum. One child died. CONCLUSION: Gastrointestinal complications of D+ HUS are rare, but they can be lethal, and early surgery may sometimes prove necessary. However, we were not able to demonstrate a correlation between the severity of the gastrointestinal manifestations and the clinical or biological signs accompanying D+ HUS.


Subject(s)
Diarrhea/complications , Gastrointestinal Diseases/etiology , Hemolytic-Uremic Syndrome/complications , Adolescent , Child , Child, Preschool , Diagnosis, Differential , Female , Follow-Up Studies , Gastrointestinal Diseases/diagnosis , Gastrointestinal Diseases/epidemiology , Humans , Incidence , Infant , Male , Prognosis , Retrospective Studies , Severity of Illness Index
3.
Therapie ; 52(5): 487-9, 1997.
Article in French | MEDLINE | ID: mdl-9501583

ABSTRACT

The main points of a workshop on the place of clinical trials in the memory clinics in France are reproduced schematically. The efficiency of these centres has been tested at the time of the numerous clinical trials performed in France on Alzheimer's disease. In parallel, several difficulties have been pointed out: inhomogeneity of the technical approaches, official role of psychologists in the hospital teams, integration of clinical research to individual care. A particular effort should be oriented towards specific research on the different types of dementia, on early stages, on information for both media and authorities as well as on specific technical and methodological problems.


Subject(s)
Memory Disorders/diagnosis , Alzheimer Disease/diagnosis , Alzheimer Disease/therapy , Clinical Trials as Topic , Evaluation Studies as Topic , France , Humans , Memory Disorders/therapy , Referral and Consultation
4.
Br J Dermatol ; 135(1): 124-7, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8776375

ABSTRACT

Omenn's reticulosis is an inherited severe combined immunodeficiency characterized by neonatal exfoliative erythroderma. A newborn baby who had minimal change nephrotic syndrome and Omenn's reticulosis is reported. Abnormalities in lymphocyte function could explain both the nephropathy and the cutaneous changes.


Subject(s)
Lymphatic Diseases/complications , Nephrotic Syndrome/complications , Severe Combined Immunodeficiency/complications , Skin Neoplasms/complications , Dermatitis, Exfoliative/complications , Humans , Infant, Newborn , Lymphatic Diseases/pathology , Male , Skin Neoplasms/pathology
5.
Neurochirurgie ; 42(1): 54-60, 1996.
Article in French | MEDLINE | ID: mdl-8763765

ABSTRACT

Organic amnesia is typically associated with lesions in either the diencephalic or medial temporal regions of the brain. However, amnesia can result from other kinds of lesions, in particular those resulting from an aneurysm of the anterior communicating artery (ACoA). In the present study, 7 patients who became amnesic following a ruptured and operated ACoA aneurysm were comparated neuropsychologically with 11 patients with ruptures but no cognitive complaints and 18 normal control subjects. They were submitted to explicit and implicit memory tests and to tests claimed to be sensitive to frontal lobe dysfunction. The performance of the 11 ACoa patients without cognitive complaints revealed evidence for a functional frontal dysfunction (test of Stroop) and a partial deficit of explicit memory (free recall and long-term recall). The performance of the 7 ACoa amnesics revealed evidence for a functional frontal dysfunction and a deficit of explicit memory (safe in recognition). Anosognosia was also observed. The performance of all patients revealed the preservation of implicit memory in procedural tasks (serial reaction time and mirror reading) as diencephalic and temporal amnesia. The functionnal nature of the syndrome is discussed.


Subject(s)
Intracranial Aneurysm/surgery , Memory Disorders/etiology , Neuropsychological Tests , Adult , Aged , Female , Humans , Intracranial Aneurysm/complications , Male , Memory Disorders/diagnosis , Middle Aged , Postoperative Period , Reaction Time
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