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199 Possible Causes for Lymphadenopathy, Peripheral Blood Smear Abnormal

  • Chronic Lymphocytic Leukemia

    Peripheral blood smear revealed leukocytosis with absolute lymphocytosis (absolute lymphocyte count: 37870 cells/mm³).[] Lymphadenopathy may or may not be present. Stage III: Absolute lymphocytosis with anemia is present. Hepatosplenomegaly and lymphadenopathy may or may not be present.[] Abnormalities may also be seen in peripheral blood smears. Treatment.[]

  • Follicular Lymphoma

    A complete blood cell count (CBC) with differential should be obtained, including examination of the peripheral blood smear if the differential is abnormal.[] The patient did not have any significant peripheral or axial lymphadenopathy, which made the diagnosis difficult in absence of histopathology.[] In our report, a 62-year-old female was initially diagnosed with a low-grade follicular lymphoma, and 2 years later she presented with bilateral lung masses and lymphadenopathy[]

  • Chronic Myelomonocytic Leukemia

    Peripheral blood smear for CMML showing abnormal cells. Chronic myelomonocytic leukemia (CMML) is an aggressive cancer of the blood that is resistant to treatment.[] CASE REPORT A 67-year-old Caucasian man, who was a long-term cigarette smoker, presented with a five-year history of leukocytosis and cervical lymphadenopathy.[] In addition, morphologic evaluation of the peripheral blood smear and T-cell gene rearrangement studies by polymerase chain reaction (PCR) were performed.[]

  • Philadelphia Chromosome Positive Chronic Myeloid Leukemia

    Petechiae, ecchymoses, and lymphadenopathy are remarkable findings on the physical exam in the later stages. The disease progresses towards a blast crisis.[] On physical examination, he had huge splenomegaly and hepatomegaly, sternal tenderness and generalized lymphadenopathy.[] A 12 -year -male child with generalized lymphadenopathy and hepatosplenomegaly had a crisis phase of presentation instead of the usual chronic phase of onset of disease.[]

  • B Acute Lymphoblastic Leukemia

    She displayed hepatosplenomegaly and pleural and abdominal effusions without lymphadenopathy. Lactate dehydrogenase (10,554 U/L; normal range 106–211 U/L) was elevated.[] (49%) 51 (51%) 57 (57%) 43 (43%) 0.257 Fever 144 (72.0%) 76 (76%) 68 (68%) 0.208 Infection 128 (64.0%) 66 (66%) 62 (%) 0.556 Bleeding 96 (48.0%) 45 (45%) 51 (51%) 0.396 Lymphadenopathy[] Lymphadenopathy, hepatomegaly, splenomegaly, arthralgia and bone pain are signs and symptoms also reported (1, 3, 6).[]

  • T-Cell Acute Lymphoblastic Leukemia

    In comparison, patients 16 to 60 years old (n 21) more commonly had an anterior mediastinal mass (8 [38%]), hepatosplenomegaly (10 [48%]), and lymphadenopathy (16 [76%]).[] […] respiratory emergency, pleural effusion Younger (age 16 - 60 years) patients compared to older (61 years) patients have more hepatosplenomegaly, present with mediastinal mass and lymphadenopathy[] Clinical examination may reveal splenomegaly and lymphadenopathy.[]

  • Primary Myelofibrosis

    Red blood cells frequently appear abnormal in myelofibrosis on a peripheral smear with unusual shapes and sizes, reflecting defective production of the red blood cells.[] Clinical manifestations depend on the type of blood cell affected and may include anemia, pallor, splenomegaly, hypermetabolic state, petechiae, ecchymosis, bleeding, lymphadenopathy[] Abdominal examination reveals splenomegaly, palpable 8 cm. below the costal margin without hepatomegaly CT scans of the chest, abdomen, and pelvis reveal moderate mediastinal lymphadenopathy[]

  • Sézary Syndrome

    Peripheral blood smear – A type of procedure wherein a blood sample is surveyed under a microscope to see whether the cells appear normally and to count circulating blood[] A 44-year-old man known to have human immunodeficiency virus (HIV) infection presented to our clinic with erythroderma, generalized lymphadenopathy, and cutaneous nodules[] We describe the case of a 17-year-old Hispanic boy who had had erythroderma and diffuse lymphadenopathy for approximately 6 months.[]

  • Thalassemia

    […] beta chain that results in microcytic hypochromic anemia, an abnormal peripheral blood smear with nucleated red blood cells, and reduced amounts of hemoglobin A.[] Medical records revealed the patient developed a fever and superficial lymphadenopathy and soft palate enlargement 8 months post-HSCT.[] It includes hemoglobin, hematocrit and more details about the red blood cells. Peripheral smear.[]

  • Chronic Eosinophilic Leukemia

    The patient was treated with imatinib at 400 mg/d with improvement of symptoms, reduction of lymphadenopathy and normalization of the eosinophil count.[] We report a case of chronic eosinophilic leukemia in a 9 year old girl who presented with anemia, thrombocytopenia, leucocytosis (mostly dysplastic eosinophils), lymphadenopathy[] Lymphadenopathy is also common with FGFR1 mutations.Infiltration of eosinophils causes organ damage.[]

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