Siham Cherkaoui
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View article: A Review of the Latest Updates in Cytogenetic and Molecular Classification and Emerging Approaches in Identifying Abnormalities in Acute Lymphoblastic Leukemia
A Review of the Latest Updates in Cytogenetic and Molecular Classification and Emerging Approaches in Identifying Abnormalities in Acute Lymphoblastic Leukemia Open
Acute lymphoblastic leukemia (ALL) is a heterogeneous hematologic malignancy defined by the uncontrolled proliferation of lymphoid precursors. Accurate diagnosis and effective therapeutic strategies hinge on a comprehensive understanding o…
View article: The first regional interdisciplinary paediatric palliative care (PPC) workshop for the Eastern Mediterranean Region: a groundbreaking collective step for PPC integration
The first regional interdisciplinary paediatric palliative care (PPC) workshop for the Eastern Mediterranean Region: a groundbreaking collective step for PPC integration Open
Amidst the global disparities in providing Paediatric Palliative Care (PPC), the compounded realities in the Eastern Mediterranean region intensify the need for palliative care for children with cancer. This region hosts 12% of children ne…
View article: Pancytopenia Revealing Medullary Granulomatosis : An Unexpected Diagnosis of Systemic Familial Sarcoidosis
Pancytopenia Revealing Medullary Granulomatosis : An Unexpected Diagnosis of Systemic Familial Sarcoidosis Open
Sarcoidosis is a granulomatous disease of unknown origin, characterized by highly variable clinical presentations. Diagnosis is based on compatible clinical features, the presence of non-caseating granulomas on biopsy, and the exclusion of…
View article: Primary Adrenal Insufficiency in Children: Adrenoleukodystrophy as a Rare Etiology in Girls
Primary Adrenal Insufficiency in Children: Adrenoleukodystrophy as a Rare Etiology in Girls Open
X-linked adrenoleukodystrophy (X-ALD) is a peroxisomal disease due to a mutation in the ABCD1 gene that leads to the accumulation of very-long-chain fatty acids in tissues. X-linked adrenoleukodystrophy (X-ALD) is a rare metabolic disorder…
View article: Ovarian relapse in a child with B-ALL: a case report
Ovarian relapse in a child with B-ALL: a case report Open
This case presents an 8-year-old girl diagnosed with B-cell acute lymphoblastic leukemia (B-ALL), who relapsed after 3 years of treatment and 1 year of complete remission, with an unusual extramedullary relapse in the ovary. Ovarian relaps…
View article: Immune Thrombocytopenic Purpura Complicated by Pituitary Apoplexy: 5th Case Worldwide
Immune Thrombocytopenic Purpura Complicated by Pituitary Apoplexy: 5th Case Worldwide Open
Background: Pituitary apoplexy (PA) is an uncommon condition that may arise as a consequence of immune thrombocytopenic purpura (ITP). It is typically observed in the context of pituitary adenoma. The condition may manifest with symptoms o…
View article: A Review of Emerging Cytogenetic and Molecular Approaches in Identifying Abnormalities in Acute Lymphoblastic Leukemia
A Review of Emerging Cytogenetic and Molecular Approaches in Identifying Abnormalities in Acute Lymphoblastic Leukemia Open
Acute Lymphoblastic Leukemia (ALL) is a diverse hematologic malignancy characterized by the uncontrolled proliferation of lymphoid precursors. A comprehensive understanding of the genetic alterations associated with ALL is crucial for accu…
View article: Amylose amyloid light-chain (AL) et lymphome folliculaire: à propos d´un cas
Amylose amyloid light-chain (AL) et lymphome folliculaire: à propos d´un cas Open
The association of light-chain (AL) amyloidosis with type B follicular lymphoma is extremely rare, as the clone secreting the amyloidogenic light chain is generally plasmacytic. We here report the case of a 67-year-old patient with no spec…
View article: t(1;4) translocation in a child with acute lymphoblastic leukemia: a case report
t(1;4) translocation in a child with acute lymphoblastic leukemia: a case report Open
Background Acute lymphoblastic leukemia is the most common childhood cancer, with an 80% frequency in children between 1 and 10 years old. The outcome and prognosis of acute lymphoblastic leukemia in children depends on various factors, su…
View article: Epidemiological and clinical characteristics of children with peripheral neuroblastic tumors: a study on a Moroccan population
Epidemiological and clinical characteristics of children with peripheral neuroblastic tumors: a study on a Moroccan population Open
View article: IBCL-328 Follicular Lymphoma: Concentric Study in the Hematology Department of the IBN ROCHD University Hospital Center
IBCL-328 Follicular Lymphoma: Concentric Study in the Hematology Department of the IBN ROCHD University Hospital Center Open
View article: HL-326 Disseminated Pediatric Hodgkin Lymphoma (HL): Concentric Study Within the Hematology Department at Ibn Rochd University Hospital
HL-326 Disseminated Pediatric Hodgkin Lymphoma (HL): Concentric Study Within the Hematology Department at Ibn Rochd University Hospital Open
View article: ALL-379 Acute Undifferentiated Leukemia: Rare Clinical Case
ALL-379 Acute Undifferentiated Leukemia: Rare Clinical Case Open
View article: HL-357 Localized Hodgkin Lymphoma (HL) in Children: Retrospective Study
HL-357 Localized Hodgkin Lymphoma (HL) in Children: Retrospective Study Open
View article: POSTER: MM-317 Non-Cryopreserved Hematopoietic Stem Cells Autotransplantation in Patients With Multiple Myeloma (MM) Aged 65 and Older
POSTER: MM-317 Non-Cryopreserved Hematopoietic Stem Cells Autotransplantation in Patients With Multiple Myeloma (MM) Aged 65 and Older Open
View article: ABCL-411 Management of DLBCL (Diffuse Large B-Cell Lymphoma): A Monocentric Experience
ABCL-411 Management of DLBCL (Diffuse Large B-Cell Lymphoma): A Monocentric Experience Open
View article: CML-294 Chronic Myeloid Leukemia of the Elderly Over 60 Years: Epidemiological, Cytogenetic, and Therapeutic Profile in CASABLANCA
CML-294 Chronic Myeloid Leukemia of the Elderly Over 60 Years: Epidemiological, Cytogenetic, and Therapeutic Profile in CASABLANCA Open
View article: IBCL-318 Epidemiological, Clinical, Histopathologic and Therapeutic Characteristics of Marginal Zone Lymphoma: Experience of the Hematology Department of Casablanca in Morocco
IBCL-318 Epidemiological, Clinical, Histopathologic and Therapeutic Characteristics of Marginal Zone Lymphoma: Experience of the Hematology Department of Casablanca in Morocco Open
View article: POSTER: IBCL-318 Epidemiological, Clinical, Histopathologic and Therapeutic Characteristics of Marginal Zone Lymphoma: Experience of the Hematology Department of Casablanca in Morocco
POSTER: IBCL-318 Epidemiological, Clinical, Histopathologic and Therapeutic Characteristics of Marginal Zone Lymphoma: Experience of the Hematology Department of Casablanca in Morocco Open
View article: POSTER: HL-357 Localized Hodgkin Lymphoma (HL) in Children: Retrospective Study
POSTER: HL-357 Localized Hodgkin Lymphoma (HL) in Children: Retrospective Study Open
View article: MM-317 Non-Cryopreserved Hematopoietic Stem Cells Autotransplantation in Patients With Multiple Myeloma (MM) Aged 65 and Older
MM-317 Non-Cryopreserved Hematopoietic Stem Cells Autotransplantation in Patients With Multiple Myeloma (MM) Aged 65 and Older Open
View article: POSTER: IBCL-417 Primary Intracranial Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue in Cerebral Localization: Case Report
POSTER: IBCL-417 Primary Intracranial Marginal Zone B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue in Cerebral Localization: Case Report Open
View article: Lymphome B diffus à grandes cellules splénique primitif : une cause rare de splénomégalie isolée
Lymphome B diffus à grandes cellules splénique primitif : une cause rare de splénomégalie isolée Open
Primary splenic non-Hodgkin lymphoma is extremely rare, characterized by isolated splenic disease without other lymphoma locations. It’s most often revealed by isolated splenomegaly. We report the case of a 43-year-old female patient with …
View article: Pain assessment and management in the Moroccan haemophilia population: a prospective descriptive study
Pain assessment and management in the Moroccan haemophilia population: a prospective descriptive study Open
Introduction For people with haemophilia (PwH) who live in developing countries, haemophilia continues to be a condition with serious medical and social consequences. In Morocco, the efforts of patient associations and medical teams have l…
View article: Epidemiology and Outcome of Primary Cerebral Lymphoma in Immunocompetent Patients: A Monocentric Study
Epidemiology and Outcome of Primary Cerebral Lymphoma in Immunocompetent Patients: A Monocentric Study Open
Primary cerebral lymphoma (PCL) is a form of extranodal non-Hodgkin’s lymphoma with a poor prognosis. Very few cohorts have been reported in the literature. It is a rare form in 1% of extranodal lymphomas, and 3% to 4% of brain tumors. The…
View article: Evaluation of Therapeutic Results of A Series of Moroccan Patients Aged 20 To 60 Years Treated According To The Acute Myeloid Leukaemia 03 Protocol At The Paediatric Haematology Oncology Centre In Casablanca
Evaluation of Therapeutic Results of A Series of Moroccan Patients Aged 20 To 60 Years Treated According To The Acute Myeloid Leukaemia 03 Protocol At The Paediatric Haematology Oncology Centre In Casablanca Open
Acute Myeloblastic Leukaemia (AML) is a malignant haemopathy characterized by infiltration and accumulation in the bone marrow by myeloblastic-type blast cells causing medullary insufficiency. At the global level, the search for improved A…
View article: Current Cytogenetic Abnormalities in Acute Myeloid Leukemia
Current Cytogenetic Abnormalities in Acute Myeloid Leukemia Open
Cytogenetic abnormalities are frequently reported in the literature describing the presence of chromosomal rearrangements in important cases of acute myeloid leukemia (AML); the rate can reach 50–60% of cases of AML. Cytogenetic abnormalit…
View article: A challenging management of hemophilia B patient with inhibitors undergoing major orthopedic surgeries in a resource‐constrained country
A challenging management of hemophilia B patient with inhibitors undergoing major orthopedic surgeries in a resource‐constrained country Open
In this paper, we report a life‐threatening condition and relate our experience in managing a hemophilia B patient who required three surgical procedures, highlighting the difficulties we encountered in our setting and propose some tangibl…
View article: Peripheral Medulloepithelioma: A Rare Entity to Know
Peripheral Medulloepithelioma: A Rare Entity to Know Open
According to the World Health Organization, medulloepithelioma belongs to the embryonal neoplasm entity. It is a very rare, highly malignant tumor typically affecting infants and young children. Usually, the tumor arises in the eye or in t…
View article: AMYLOSE CONJONCTIVALE: PREMIERE MANIFESTATION D’UNE AMYLOSE SYSTEMIQUE ASSOCIEE AU MYELOME MULTIPLE
AMYLOSE CONJONCTIVALE: PREMIERE MANIFESTATION D’UNE AMYLOSE SYSTEMIQUE ASSOCIEE AU MYELOME MULTIPLE Open
Introduction L’amylose systémique de type AL a été décrite dans presque tous les organes. Cependant l’atteinte conjonctivale est relativement rare et décrite le plus souvent sous forme de cas isolés et petites séries de cas. Elle est le pl…