scholarly journals Non-Hodgkin Lymphoma Associated Eczema and Prurigo Nodularis: A Case Report

2018 ◽  
Vol 12 (2) ◽  
pp. 107-109
Author(s):  
Mehdi Iskandarli ◽  
İlgen Ertam ◽  
Banu Yaman
Keyword(s):  
Case Report ◽  
Hodgkin Lymphoma ◽  
Prurigo Nodularis ◽  
Non Hodgkin Lymphoma

Osmotic demyelination syndrome in patients with non-Hodgkin lymphoma: A case report and literature review

2021 ◽  
pp. 1-6
Author(s):  
Miguel García-Grimshaw ◽  
Amado Jiménez-Ruiz ◽  
José Luis Ruiz-Sandoval ◽  
Carlos Cantú-Brito ◽  
Erwin Chiquete
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Hodgkin Lymphoma ◽  
Osmotic Demyelination Syndrome ◽  
Non Hodgkin Lymphoma ◽  
Osmotic Demyelination

scholarly journals Primary small cell type of non-Hodgkin lymphoma of the colon: a case report

2020 ◽  
Vol 14 (1) ◽  
Author(s):  
Eyal Meir ◽  
Chovav Handler ◽  
Uri Kaplan ◽  
Doron Kopelman ◽  
Ossama A. Hatoum
Keyword(s):  
Case Report ◽  
Hodgkin Lymphoma ◽  
Small Cell ◽  
Primary Lymphoma ◽  
Cell Type ◽  
Rare Type ◽  
Case Presentation ◽  
Carcinoma Of The Colon ◽  
Non Hodgkin Lymphoma ◽  
High Level

Abstract Introduction Primary lymphoma of the colon is exceedingly rare and comprises 0.2–1% of all colon tumors. The most common subtype of lymphoma in the colon is non-Hodgkin lymphoma. Symptoms are often nonspecific, and treatment varies between chemotherapy alone and a combination of surgery and chemotherapy. Case presentation We describe a case of a Ashkenazi Jew patient who presented in the typical way that carcinoma of the colon might present but turned out to have a very rare type of tumor in both its histology and its location. Conclusion There was apparent discordance between the relative bulkiness and gross appearance of the tumor with the unrevealing result of the biopsies, demanding a high level of suspicion as to the actual presence and possible type of such a tumor in the future.

scholarly journals Tyrosine kinase inhibitor and rituximab-CHOP treatment for concurrent chronic myeloid leukemia and non-Hodgkin lymphoma: a case report

2017 ◽  
Vol 5 (12) ◽  
pp. 2047-2050
Author(s):  
Yuki Takeyasu ◽  
Atsushi Satake ◽  
Yoshiko Azuma ◽  
Yukie Tsubokura ◽  
Hideaki Yoshimura ◽  
...  
Keyword(s):  
Case Report ◽  
Chronic Myeloid Leukemia ◽  
Tyrosine Kinase ◽  
Tyrosine Kinase Inhibitor ◽  
Hodgkin Lymphoma ◽  
Myeloid Leukemia ◽  
Kinase Inhibitor ◽  
Non Hodgkin Lymphoma

Oral Manifestation of NK/T-Cell Non-Hodgkin Lymphoma: A Case Report

2015 ◽  
Vol 120 (2) ◽  
pp. e69
Author(s):  
DANIEL CAMPANHÃ ◽  
JOYCE GIMENEZ MENON ◽  
LETÍCIA OLIVEIRA TONIN ◽  
ISABELA WERNECK DA CUNHA ◽  
GARLES MILLER MATIAS VIEIRA ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Hodgkin Lymphoma ◽  
Oral Manifestation ◽  
Non Hodgkin Lymphoma ◽  
Nk T Cell

Granulomatous panuveitis associated with Hodgkin lymphoma: A case report with review of the literature

2020 ◽  
pp. 112067212096903
Author(s):  
Abdulaziz A Alshamrani ◽  
Waleed K Alsarhani ◽  
Abdulrahman A Aljasser ◽  
Marcos J Rubio-Caso
Keyword(s):  
Case Report ◽  
Hodgkin Lymphoma ◽  
Pigment Epithelium ◽  
Retinal Pigment ◽  
Clinical Signs ◽  
Cervical Lymphadenopathy ◽  
Intraocular Lymphoma ◽  
Review Of The Literature ◽  
Diagnostic Challenge ◽  
Non Hodgkin Lymphoma

Background: Intraocular lymphoma (IOL) is an uncommon ophthalmic malignancy and poses a diagnostic challenge. Uveitis associated with systemic lymphoma (USL) has been predominantly attributed to non-Hodgkin lymphoma (NHL) and rarely reported with Hodgkin lymphoma (HL) in the literature. Methods: Case report with review of the literature. Results: A 25-year-old healthy male presented with bilateral granulomatous panuveitis including vasculitis and discrete chorioretinal yellowish-white lesions. Macular optical coherence tomography (OCT) of both eyes revealed a disruption of ellipsoid and interdigitation zones over the areas of subretinal lesions as well as a small sub-retinal pigment epithelium (RPE) deposit in one eye. Thorough uveitis workup revealed clavicular, axillary and cervical lymphadenopathy, and biopsy of lymph nodes confirmed the diagnosis of nodular lymphocyte-predominant (NLP) HL. Six months later and after receiving chemotherapy, all symptoms and most of clinical signs resolved. Conclusions: Clinical features of USL do not differ between HL and NHL. However, the age of presentation may be much younger in HL. Ocular manifestations can precede systemic HL diagnosis, as shown in our patient. Therefore, USL should be part of the differential diagnosis of panuveitis. Paraneoplastic inflammation is thought be the cause of uveitis associated with HL. The sub-RPE deposit and disruption of ellipsoid and interdigitation zones on OCT have not been documented before as a manifestation of uveitis secondary to HL. In addition, the NLP subtype of HL was reported in only 1 case with uveitis in the literature.

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