CD3+/CD4+/CD5+/CD8+/CD21+/CD34-/CD45-/CD79a-/TCRαβ+/TCRγδ-/MHCII+ T-zone lymphoma in a dog with generalized lymphadenopathy: a case report

Lymphoma can present with different type of serous effusion like pleural, pericardial and ascites and it signifies poor outcome .Pleural effusions are the most common type among these. Ascites and pericardial effusion are rare. Effusion can be can be caused by direct infiltration and impairment of the lymphatic drainage .Several investigations are available like study of the fluid for cytological, biochemical, immunohistochemistry and cytogenetics study to assess the qualities of effusion and make a quick diagnosis. This present case report will describe a case of 40 year old female patient with non-Hodgkin’s lymphoma (NHL) presented with generalized lymphadenopathy and chylous ascites and pleural effusion. Bangladesh Med J. 2018 May; 47 (2): 38-40

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CANDLE Syndrome: Case Report of a Rare Type of Auto- Inflammatory Disease

Bangladesh Journal of Child Health ◽

10.3329/bjch.v44i3.52711 ◽

2021 ◽

Vol 44 (3) ◽

pp. 174-177

Author(s):

Md Asif Ali ◽

Mohammad Imnul Islam ◽

Shahana Akhtar Rahman

Keyword(s):

Case Report ◽

Autoinflammatory Disease ◽

Failure To Thrive ◽

Skin Lesions ◽

Recurrent Fever ◽

Rare Type ◽

Auto Inflammatory Disease ◽

Laboratory Investigations ◽

Generalized Lymphadenopathy ◽

Psmb8 Gene

CANDLE syndrome (chronic atypical neutophilic dermatosis with lipodystrophy and elevated temperature) is an autoinflammatory disease/syndrome characterized by recurrent fever, skin lesions, and multisystem inflammatory manifestations. Most of the patients have shown mutation in PSMB8 gene. Here, we report a 9-year-old girl with recurrent fever, atypical facies, widespread skin lesions, generalized lymphadenopathy, hepato-splenomegaly, lipodystrophy, and failure to thrive. Considering the clinical features and laboratory investigations including skin biopsy findings, diagnosis was consistent with CANDLE syndrome. Therefore, it is recommended to consider CANDLE syndrome in a young child who presents with recurrent fever, characteristics rashes, organomegaly and failure to thrive. Bangladesh J Child Health 2020; VOL 44 (3) :174-177

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Prostatic Adenocarcinoma Incognito Manifestation as Generalized Lymphadenopathy: a Rare Case Report

Indian Journal of Surgical Oncology ◽

10.1007/s13193-016-0558-5 ◽

2016 ◽

Vol 8 (1) ◽

pp. 91-93

Author(s):

Amit Sehrawat ◽

Satyanker Gupta ◽

Tiwari Alok

Keyword(s):

Case Report ◽

Rare Case ◽

Prostatic Adenocarcinoma ◽

Rare Case Report ◽

Generalized Lymphadenopathy

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Generalized Lymphadenopathy as Presenting Feature of Systemic Lupus Erythematosus: Case Report and Review of the Literature

Journal of Clinical Medicine Research ◽

10.14740/jocmr2717w ◽

2016 ◽

Vol 8 (11) ◽

pp. 819-823 ◽

Cited By ~ 4

Author(s):

Wais Afzal ◽

Talal Arab ◽

Tofura Ullah ◽

Katerina Teller ◽

Kaushik J. Doshi

Keyword(s):

Systemic Lupus Erythematosus ◽

Case Report ◽

Lupus Erythematosus ◽

Review Of The Literature ◽

Systemic Lupus ◽

Systemic Lupus Erythematosus Case ◽

Generalized Lymphadenopathy

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Rosai-Dorfman Disease Complicated by Autoimmune Hemolytic Anemia in a Child: A Case Report and Review of the Literature

Case Reports in Oncology ◽

10.1159/000485968 ◽

2018 ◽

Vol 11 (1) ◽

pp. 55-62 ◽

Cited By ~ 4

Author(s):

Amer A. Lardhi ◽

Abdullah K. Al-Mutairi ◽

Mohammed H. Al-Qahtani ◽

Atheer K. Al-Mutairi

Keyword(s):

Case Report ◽

Hemolytic Anemia ◽

Autoimmune Hemolytic Anemia ◽

Female Child ◽

Infectious Agents ◽

Review Of The Literature ◽

Massive Lymphadenopathy ◽

Rosai Dorfman Disease ◽

Generalized Lymphadenopathy

Rosai-Dorfman disease is a rare histiocytic proliferative disorder that commonly presents with a massive lymphadenopathy and a variety of constitutional symptoms. Severe hemolytic anemia is an infrequent complication of this disease. Although the etiology of the condition is unknown, infectious agents including viruses have been implicated. We describe a 2-year-old female child who presented with fever, pallor, and generalized lymphadenopathy complicated by the development of autoimmune hemolytic anemia. A review of the literature of this condition is also provided.

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Digital gangrene as an unusual paraneoplastic manifestation of hodgkins lymphoma—a rare case report

The Egyptian Journal of Internal Medicine ◽

10.1186/s43162-021-00076-7 ◽

2021 ◽

Vol 33 (1) ◽

Author(s):

Swaroopa Deme ◽

Bhaskar Kakarla ◽

Venkateswar Rao P. ◽

Raju YSN ◽

Nageswara Rao M.

Keyword(s):

Case Report ◽

Hodgkin’S Lymphoma ◽

Ring Finger ◽

Middle Finger ◽

Hodgkin's Lymphoma ◽

Severe Thrombocytopenia ◽

Digital Ischemia ◽

Rare Case Report ◽

Generalized Lymphadenopathy ◽

The Right

Abstract Background Hodgkin’s lymphoma presenting with digital ischemia and gangrene is a rare manifestation. Paraneoplastic manifestations are rare in Hodgkin’s lymphoma but can occur in the form of paraneoplastic cerebellar degeneration (PCD) and dermatomyositis/polymyositis. This case report adds an exceptional presentation of Hodgkin's lymphoma as digital ischemia and gangrene. Case presentation We report a case of a 60-year-old male patient who presented with fever, cough, shortness of breath, the pain in the right middle finger. On examination bluish-black discoloration of the right middle finger, left middle finger, ring finger, and generalized lymphadenopathy was noted. On further evaluation, he was found to have anemia, eosinophilia, and severe thrombocytopenia with a normal coagulation profile and negative rheumatological workup. Arterial Doppler of both upper limbs showed the normal study. He was diagnosed to have Hodgkin’s lymphoma on the lymph node and bone marrow biopsy. He was started on chemotherapy with partial improvement in symptoms and was lost to follow-up after 2 cycles. Conclusions Digital ischemia can be a rare paraneoplastic manifestation of Hodgkin’s lymphoma.

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