Publications by authors named "Mseddi Sondes"

We report a case of Lymphocytic Lymphoma presenting with primary manifestation in the prostate. A 82 year-old man presented to emergency department with acute urinary retention. Digital rectal examination revealed a voluminous and firm prostate.

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Background: Gaucher disease (GD) is the most frequent lysosomal storage disorder; type 1 is by far the most common form. It is characterized by variability in age of onset, clinical signs and progression. It is usually diagnosed in the first or second decade of life with the appearance of bone pains, splenomegaly and thrombocytopenia, but the disease may be diagnosed at any age between 1 and 73 years.

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Subacute necrotizing lymphadenitis or Kikuchi-Fujimoto disease is a benign pathological entity diagnosed chiefly in young adults. We report a case in a 20-year-old woman who presented with swollen lymph nodes and a fever. Disseminated lymphadenopathy with nodes measuring up to 6 cm in diameter was found upon physical examination.

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Plasma cell leukemia is considered as the leukemic variant of multiple myeloma. It is a rare entity. There are two forms: a secondary one following a known myeloma, the diagnosis of which is easy, and a primary one arising without a preceding phase of multiple myeloma.

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Introduction: Glanzmann's thrombasthenia (GT) is a rare congenital thrombopathy, with a recessive autosomal transmission. We present here the genealogic study of a series of patients suffering from GT.

Patients And Methods: This is a retrospective study about all the GT patients treated in Sfax hematology department during 18 years.

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Article Synopsis
  • Gaucher's disease is a rare inherited condition caused by low levels of the enzyme beta glucocerebrosidase, leading to health issues like bone pain and enlarged spleen.
  • Symptoms typically appear in younger patients, but misdiagnosis can occur, especially if the spleen isn't visibly enlarged.
  • This report discusses two older patients, 70 and 46 years old, who were unexpectedly diagnosed with Gaucher's disease during a bone marrow examination while being checked for low blood cell counts.
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In this report, we studied the frequency, the types and the prognosis value of the Durie and Salmon's classification of radiological bone lesions in multiple mycloma. Our study concerned 52 patients presenting multiple myeloma, defined according to South West Oncology Group criteria, collected during nine years (1988-1996). Radiological anomalies were noted in 89% of the cases.

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