Intravascular large B-cell lymphoma diagnosed at autopsy

نویسندگان

چکیده

Background: Intravascular large B-cell lymphoma is a rare, extranodal characterised by intravascular growth of malignant mature population, primarily affecting capillaries. Pre-mortem diagnosis can be challenging as patients often present with non-specific clinical findings including fever unknown origin, decreased general condition and neurological abnormalities. Radiological may or falsely negative. Aims: We the case an 87-year-old lady who presented to hospital cognitive functional decline, headache presumed transient ischaemic attacks. Despite extensive investigations definitive cause for her symptoms was unable established prior death. Autopsy revealed multiorgan involvement lymphoma. Methods: The patient underwent full non-coronial autopsy. With consent, patient’s brain retained extended fixation neuropathological assessment which also widespread lymphomatous infiltration. Results conclusions: This demonstrates rare diagnosed at autopsy highlights difficulties in pre-mortem due presentation lack diagnostic radiological features.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Intravascular large B-cell lymphoma diagnosed at renal biopsy

A 77-year-old woman was referred with renal impairment—serum creatinine 230 mmol/L (2.61 mg/dL) and proteinuria 2.14 g/day. The past medical history included hypertension, sicca symptoms and osteoarthritis. Her medications included amlodipine 5 mg od, omeprazole 20 mg od and prednisolone 10 mg od. Systematic enquiry revealed lethargy and 6 kg weight loss over 6 months. Examination was unremarka...

متن کامل

Intravascular Large B-cell Lymphoma: A Report of Two Cases

One of the rare variants of extranodal large B-cell lymphoma is intravascular large B-cell lymphoma (IVLBCL). Characteristics of IVLBCL include intraluminal selective proliferation of atypical lymphoid cells in small to medium-sized vessels. The etiologic of IVLBCL is unknown, but due to the growth pattern of this tumor, it is speculated that IVLBCL is caused by a defect in homing receptor of t...

متن کامل

Intravascular Large B-Cell Lymphoma

Case Presentation. A 69-year-old Hispanic male, with a past history of diabetes and coronary disease, was admitted for fever, diarrhea, and confusion of 4 weeks duration. Physical examination showed a disoriented patient with multiple ecchymoses, possible ascites, and bilateral scrotal swelling. Hemoglobin was 6.7, prothrombin time (PT) 21.4 seconds with international normalized ratio 2.1, part...

متن کامل

Relapsed intravascular large B-cell lymphoma

which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. A 44-year-old woman presented with myalgia and fever. Initial laboratory results were: White blood cell (WBC) count, 7.8×10 9 /L; hemoglobin, 11.3 g/dL; platelet count, 42×10 9 /L; and lactate dehydrogenase, 619 IU/L. Peripheral blood cell morphology showed ...

متن کامل

Asian-variant intravascular large B-cell lymphoma.

Intravascular large B-cell lymphoma (IVLBCL) is a rare and deadly malignancy involving the growth of lymphoma cells within vessel lumina of all organ types. IVLBCL is further divided into the hemophagocytic Asian variant and a classical Western variant. Both variants are difficult to diagnose by imaging, and although diagnostic criteria have been developed to guide workup, histopathological exa...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Pathology

سال: 2023

ISSN: ['1465-3931', '0031-3025']

DOI: https://doi.org/10.1016/j.pathol.2022.12.154