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lymphadenopathy/edema
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Pagina 1 a partire dal 541 risultati
Atypical hyaline vascular-type castleman's disease with thrombocytopenia, anasarca, fever, and systemic lymphadenopathy.
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Recently, atypical Castleman's disease (CD) was reported in Japan. This disease is considered as TAFRO syndrome or non-idiopathic plasmacytic lymphadenopathy (IPL), a constellation of clinical symptoms, namely, thrombocytopenia, anasarca, fever, reticulin fibrosis, and organomegaly without
Unusual presentation of prostate cancer with generalized lymphadenopathy and unilateral leg edema.
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Prostate cancer most often metastases to bones and regional lymph nodes. Disseminated metastasis to distant lymph nodes is very rare. We report a case presenting with generalized lymphadenopathy and related left leg edema without any urinary symptoms and finally diagnosed as prostate cancer.
[Thoracic lymphadenopathy due to vascular transformation of lymph node sinuses associated with upper limb edema in a chronic hemodialysis patient with congestive heart failure].
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BACKGROUND
Vascular transformation of lymph node sinuses (VTLS) is a rare disorder characterized by transformation of lymph node sinuses into endothelium-lined capillary-like channels. This phenomenon was originally discovered by accident whilst examining regional lymph nodes draining cancer.
A man with chronic leg edema, purpuric skin lesions, and abdominal lymphadenopathy.
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Diffuse lymphadenopathy and anasarca in a 65-year-old woman.
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[Chronic edema of the lower extremities evolving for 2 years. Bilateral inguinal adenopathy caused by mapighian metastasis. Discovery of a latent, probably metastatic, anorectal epithelioma].
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[Edema and lymphadenopathy. 55-year-old patient with edema and lymphadenopathy: significance of fine needle biopsy. Metastatic large cell undifferentiated carcinoma of unknown primary tumor (pancreas, stomach, bronchial differential diagnosis)].
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A case of multicentric castleman's disease of mixed-type, which showed constellation of symptoms, i.e., thrombocytopenia, anasarca, anemia, fever, myelofibrosis, and lymphadenopathy.
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POEMS syndrome presenting with abdominal distension, lower limb edema and shortness of breath: A case report and literature review.
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POEMS syndrome is a rare paraneoplastic disorder. A 60-year-old female patient was admitted to the Department of Gastroenterology, Xiangya Hospital of Central South University (Changsha, China), complaining of abdominal distension, severe edema of both lower limbs and shortness of breath for more
Bilateral eyelid edema: an uncommon presentation of Rosai-Dorfman disease.
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OBJECTIVE
Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is a rare entity with ophthalmic manifestations in 11% of patients. Orbital and eyelid involvement as the presenting features is even more unusual.
METHODS
The authors report the clinical findings of a 41-year-old man
Balanoposthitis and Penile Edema: Atypical Manifestations of Primary Syphilis.
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The typical finding in primary syphilis stage is a unique, painless chancre with indurated borders. We report a case of primary syphilis presenting as erosive and crusted balanoposthitis with an underlying chancre, penile edema, and bilateral inguinal lymphadenopathy in a heterosexual man.
Scleral nodule and bilateral disc edema as a presenting manifestation of systemic sarcoidosis.
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OBJECTIVE
To report a rare presentation of a large scleral nodule with bilateral disc edema as the initial manifestation of sarcoidosis.
METHODS
Retrospective interventional case report.
RESULTS
A 58-year-old woman was referred for evaluation of nodular scleritis. Slit-lamp examination showed a
A Patient With Toxoplasmosis as a Cause of Submental Lymphadenopathy.
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Submental mass secondary to toxoplasmosis is a rare condition and physicians rarely consider its diagnosis. The presented case reports a 43-year-old woman referred with a constant, painless, edema located in the submental area for 2 weeks. Diagnosis of toxoplasmosis was established by the positive
Adenopathy and extensive skin patch overlying a plasmacytoma with unusual histologic findings in a patient with polyneuropathy, organomegaly, endocrinopathy, monoclonal protein and skin changes syndrome and Castleman disease.
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A 56-year-old previously healthy man presented to the dermatology clinic with a 2-year history of an expanding, violaceous, infiltrated plaque on the right flank. Biopsy revealed a diffuse dermal vascular proliferation of bland, capillary-sized vessels admixed with conspicuous fibrohistiocytic cells
Pediatric lymphedema caused by diffuse cervical lymphadenopathy: A case report and review of the literature.
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Pediatric head and neck lymphedema is rare and there have not been any reported cases in children. Here we discuss severe, diffuse head and neck lymphedema in a child caused by compression of the internal jugular veins by lymphadenopathy from Kawasaki's disease. With steroid and intravenous
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