An unusual case of disseminated lymphadenopathy.

نویسندگان

  • Louise Zhou
  • Cristian Landa
  • Robert Zaiden
چکیده

A 54-year-old Caucasian female was admitted for fevers, night sweats, decreased appetite, weight loss of 20 pounds in 1 month, diffuse rash, and purpuric lesions on her lower extremities. Physical examination revealed a diffuse maculopapular rash on the anterior chest and trunk and a palpable, 1-cm, inguinal lymph node. Initial laboratory studies revealed hemoglobin of 9.1 g/dL, hematocrit of 28.4%, white blood count of 10.6 × 103/μL, platelet count of 486,000/μL, C-reactive protein of 224.3 mg/L, erythrocyte sedimentation rate of 88 mm/hr, and serum lactate dehydrogenase of 257 U/L. Normal results were found in analysis of rapid plasma regain, blood cultures, rheumatoid factor, antinuclear antibody, direct Coombs test, cytoplasmic antineutrophil cytoplasmic antigen (ANCA), perinuclear staining ANCA, atypical perinuclear ANCA, cancer antigen 125, and carbohydrate antigen 19-9. HIV testing was negative. Computed tomography (CT) with contrast of the chest, abdomen, and pelvis revealed extensive mediastinal, retroperitoneal, periaortic, pelvic, and inguinal lymphadenopathy. An inguinal lymph node biopsy and bone marrow biopsy showed no evidence of lymphoma. The right inguinal lymph node biopsy revealed granulomatous inflammation and caseating necrosis. The

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Primary Fallopian Tube Cancer: An Unusual Case of Inguinal Lymphadenopathy

Background: Primary fallopian tube cancers (PFTCs) are rare gynecological malignancies by the prevalence of 0.3-1%. The PFTCs occur in individuals within the age range of 18-88 years, more specifically at the age range of 40-65 years with the mean age of 55 years. The PFTC usually is observed with the chronic inflammation of the fallopian tube, infertility, tuberculous salpingi...

متن کامل

Kimura’s Disease – An Unusual Presentation

Introduction: Kimura’s disease is a rare chronic inflammatory disease of unknown etiology, presenting as painless subcutaneous nodules with lymphadenopathy and peripheral eosinophilia, mainly disturbing the head and neck region. It mainly affects Asian males in their 2nd to 4th decade of life. One such case of Kimura’s disease, which is uncommon in Indian natives, is reported.   Case Report: A ...

متن کامل

An Unusual Case of Hepatosplenomegaly with Cytopenia

Autoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder of immune dysregulation secondary to defective lymphocyte apoptosis. This leads to uninhibited proliferation of lymphoid tissue manifesting with lymphadenopathy, hepatosplenomegaly, autoimmune cytopenia, and an increased risk of lymphoid malignancy. We report a 2 year old boy with fever, generalized lymphadenopathy, he...

متن کامل

Cytodiagnosis of disseminated histoplasmosis in an immunocompetent individual with molluscum contagiosum-like skin lesions and lymphadenopathy

Disseminated histoplasmosis is caused by the dimorphic fungus Histoplasma capsulatum (H. capsulatum). The early clinical manifestations are nonspecific, often lead to diagnostic difficulty, and is misdiagnosed as tuberculosis and seen usually in immunosuppressed states. Fine needle aspiration cytology (FNAC) is a simple, safe, and quick technique to establish the initial diagnosis of H. capsula...

متن کامل

An unusual cause of widespread lytic bone lesions caused by sarcoidosis.

We present a case of a 59 year old asymptomatic lady who was found to have incidental findings of pulmonary, osseous and hepatic involvement with sarcoidosis. The osseous lesions were lytic and involved unusual sites such as the vertebrae and skull base. The initial clinical concern had been of multiple myeloma or disseminated metastases. Biopsy of material obtained following mediastinoscopy re...

متن کامل

A 5-year old male with “leukemic form” of disseminated post-transplant lymphoproliferative disorder

Post-transplant lymphoproliferative disorder (PTLD) represents an abnormal lymphoid proliferation that occurs in recipients of solid organ or bone marrow allograft. It includes a diverse group of diseases ranging from polymorphic B-cell hyperplasia to frank malignant lymphoma. Clinical presentation is variable, ranging from asymptomatic to generalized lymphadenopathy, mononucleosis-like syndrom...

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

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

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Clinical advances in hematology & oncology : H&O

دوره 10 1  شماره 

صفحات  -

تاریخ انتشار 2012