scholarly journals Primary Splenic Lymphoma (PSL): A Rare Presentation of Lymphoma

2018 ◽  
Vol 9 (2) ◽  
pp. 152-153
Author(s):  
Md Mahmudur Rahman Siddiqui ◽  
Md Mostafizur Rahman ◽  
Md Hasan Ali Masum ◽  
Abdul Wohab Khan ◽  
Md Ehteshamul Haque ◽  
...  

Primary Splenic Lymphoma (PSL) is a rare neoplasm of the spleen. PSL is generally presented as B cell non-Hodgkin lymphoma. Primary involvement of the spleen by lymphoma is much less common than secondary involvement. It usually presents with nonspecific symptoms like left upper abdominal pain or discomfort due to splenomegaly, pyrexia, weight loss, night sweats and weakness. In this article, we are reporting a case of PSL in a 23 years old boy who presented with splenomegaly and non-specifc symptoms.Anwer Khan Modern Medical College Journal Vol. 9, No. 2: Jul 2018, P 152-153

Author(s):  
Héctor Vergara-Miranda ◽  
Luis Adrián Alvarez-Lozada

Primary splenic lymphomas involve the spleen and/or its lymph nodes. They represent <1% of lymphomas and they imply a diagnostic challenge due to its poor symptomatology and low prevalence. There for, the objects this work describe the management and evolution of a patient with HIVAIDS and presentation of a primary lymphoma of the spleen. In this report we present the case of a 52-year-old male patient with HIV infection without treatment presented with abdominal pain, fever and a 2-month weight loss. The pre-operative computed tomography showed splenomegaly and hypodense lesions suspected to be tumoral. He was operated on, performing an exploratory laparotomy, performing an splenectomy. The histopathological study reported a non-Hodgkin lymphoma. Primary splenic lymphoma is a non frequent entity. It is necessary to be acquainted with it in order to suspect it.


2015 ◽  
Vol 23 (1) ◽  
pp. 121-123
Author(s):  
Khan Abul Kalam Azad ◽  
Md Uzzwal Mallik ◽  
Mohammad Zaid Hossain ◽  
Abdullah Shayekh ◽  
ASM Moinul Alam ◽  
...  

Pulmonary tuberculosis is one of the commonest infectious diseases in developing countries including Bangladesh. Hepatic involvement is common in disseminated tuberculosis which may be symptomatic or asymptomatic. But isolated hepatic TB without any symptoms is a rare presentation. We report a case of isolated hepatic TB in a 40 year old housewife who presented with low grade fever, vague abdominal pain and weight loss. She had no pulmonary or hepatic complains. We diagnosed the case when ultrasonogram of abdomen showed multiple space occupying lesions from where FNAC was done and sent for histopathology and Z-N staining and revealed hepatic TB. DOI: http://dx.doi.org/10.3329/jdmc.v23i1.22706 J Dhaka Medical College, Vol. 23, No.1, April, 2014, Page 121-123


2018 ◽  
Vol 154 (3) ◽  
pp. e14-e15 ◽  
Author(s):  
Dalbir S. Sandhu ◽  
Andrew M. Bellizzi ◽  
Rami El Abiad

2012 ◽  
Vol 20 (2) ◽  
pp. 124-133 ◽  
Author(s):  
MH Sardar ◽  
MAR Howdar ◽  
MU Malik ◽  
AM Appolo ◽  
MS Islam ◽  
...  

DOI: http://dx.doi.org/10.3329/jdmc.v20i2.10538 J. Dhaka Med. Coll. 2011; 20(2): 124-133


Blood ◽  
1995 ◽  
Vol 85 (8) ◽  
pp. 2000-2004 ◽  
Author(s):  
AC Wotherspoon ◽  
TM Finn ◽  
PG Isaacson

Characteristic chromosomal aberrations have been associated with subtypes of non-Hodgkin's lymphoma with distinct clinicopathologic features. Low-grade B-cell lymphomas of mucosa-associated lymphoid tissue (MALT) form such a group and might be expected to be characterized by a specific cytogenetic abnormality. Metaphase analyses of MALT lymphoma are rare due to problems with fresh tissue collection and poor in vitro proliferation. However, the small number of published series suggests that chromosome trisomies, particularly trisomy 3, might be characteristic of these tumors. The application of interphase cytogenetic techniques to routinely processed material allows the examination of a large series of archival cases and is particularly useful for the demonstration of chromosome trisomies. We have used this technique to analyze 70 cases of low-grade MALT lymphoma from various sites and found trisomy 3 in 60%. This finding compares with 16% in low-grade nodal B-cell lymphoma and 27% in primary splenic lymphoma of marginal zone type (splenic lymphoma with villous lymphocytes). These results provide further evidence that low-grade MALT lymphomas from all sites form a single pathologic entity distinct from nodal B-cell lymphomas. Although MALT lymphoma and primary splenic lymphoma may arise from marginal zone B cells, they are genetically distinct.


2021 ◽  
Vol 14 (9) ◽  
pp. e243492
Author(s):  
Ying Chen ◽  
Camelia Ciobanu ◽  
Laurel Mohrmann

We report the case of a 29-year-old man who presented with progressive weight loss, night sweats, abdominal pain and pruritus who was found to have obstructive jaundice and cholestatic pattern of liver injury on laboratory workup. Though findings on magnetic resonance cholangiopancreatography were initially concerning primary sclerosing cholangitis, he was ultimately diagnosed with biliary sarcoidosis after a liver biopsy. This case brings attention to the rare phenomenon of hepatic sarcoidosis causing hyperbilirubinemia and highlights the importance of reaching the correct diagnosis early, as the patient’s symptoms improved after initiation of steroids.


2021 ◽  
Vol 2 (6) ◽  
pp. 6-9
Author(s):  
Leonid I. Dvoretsky ◽  
◽  
Oleg E. Lutsevich ◽  
Vasilii V. Filippov ◽  
Sergei S. Golubev ◽  
...  

The case of primary splenic lymphoma, the uncommon type of non-Hodgkin lymphoma presenting with prominent splenomegaly, is reported. The disease is characterized by long asymptomatic stage and splenic abscess found during splenectomy.


Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4095-4095
Author(s):  
Robyn Scherber ◽  
Amylou Dueck ◽  
Peter L. Johansson ◽  
Tiziano Barbui ◽  
Giovanni Barosi ◽  
...  

Abstract Abstract 4095 Background: Symptomatic burden in myeloproliferative neoplasms (MPNs) is present in over 70% of MPN patients (Mesa et. al. Cancer 2007). We sought to validate a broadly applicable instrument (MPN-SAF) to assess symptoms in myelofibrosis (MF), essential thrombocythemia (ET) and polycythemia vera (PV). Methods: Using the previously validated MF-SAF as a base instrument, we added several key additional symptoms previously identified as present in all subtypes of MPNs including headaches, concentration, dizziness, extremity tingling, insomnia, sexual problems and mood changes on a 0 (absent) to 10 (worst-imaginable) scale. Validation: The MPN-SAF was administered jointly with the EORTC-QLQ-C30 as the co-validation instrument using prospective cohorts in the USA, Sweden and Italy. The translated MPN-SAF (Swedish and Italian) was created through a standard approach using teams of 4 translators working in concert. Results: Compiled MPN-SAF: Patient data: 402 MPN-SAF surveys were administered (English (25%), Italian (46%) and Swedish (28%)) in 161 ET patients (40%), 145 PV patients (36%), and 96 MF patients (24%), an average of 7.8 years (range 0 – 43 years) from their MPN diagnosis. Participants were of typical age (64.9, range 26 – 91 years) and gender (53% female) characteristic of disease. Prior hemorrhage (10%) and thrombosis (25%) were frequent. 68% of patients currently received cytoreductive therapy and 84% received cytoreductive therapy in the past. Patients and Symptomatic Burden: 19 items assessed in the MPN-SAF demonstrated consistently that the most common symptoms were fatigue (93%), decreased quality of life (84%), insomnia (65%), sad mood (65%), and sexuality problems (58%). The least common symptoms (<50% prevalence) were fevers (20%), weight loss (35%), abdominal pain (46%), cough (46%), headache (48%), and bone pain (49%). Symptoms were most severe in MF, followed by PV, then ET patients. Although symptoms are present in all 3 MPN subgroups, itching is notably more burdensome in PV patients (65%, median score of 2.8 out of 10). Additionally, abdominal pain, abdominal discomfort, early satiety and inactivity all are most prevalent and severe in MF. Interestingly, night sweats (present in 56%) overall had similar prevalence and severity across all 3 MPNs. The majority found the MPN-SAF easy to understand (98%) and “addressed most of my MPN symptoms” (96%). Comparison to EORTC-QLQ-C30: Strong correlations existed between individual items represented on both the MPN-SAF and the EORTC-QLQC30 including pain, fatigue, appetite and insomnia (all p<0.001). Additionally key symptomatic elements were highly correlated with the EORTC QLQ-C30 functional subscales. Comparison to Physician Perceptions: Comparison of the results of the MPN-SAF to enrolling physicians' blinded opinion of patients symptoms (6 assessed - night sweats, fevers, fatigue, weight loss, bone pain, and pruritus) showed excellent correlation with corresponding patients' responses except bone pain (all p<0.001). Comparison across Countries: When controlling for MPN subtype, responses between the three different countries (and 3 different languages the MPN-SAF was administered) demonstrated great consistency and correlation for all but 1 item, bone pain. Serial MPN-SAF Results: 51 patients in the USA (ET (17.6%), PV (25.5%), and MF (56.9%)), responded to a repeat MPN-SAF survey sent via US mail (50% response rate, mean time between surveys 190±63 days (range 43 – 257)). Pearson correlations indicate that most MPN-SAF items are well correlated (r >0.5, p<.001) upon repeat survey administration. Items characteristic of advanced disease, including weight loss, fever, and cough displayed lower Pearson correlations (r=0.46, -0.08, and 0.38 respectively). Intra-class correlations for test-retest reliability indicated that common features of disease, including mean BFI, inactivity, insomnia, and night sweats, were highly reproducible upon serial survey administration (ICC>0.7, 2, k model used). Conclusion: The MPN-SAF is comprehensive and reliable instrument which is available in multiple languages to evaluate MPN-associated symptoms. The MPN-SAF is recommended as a uniform symptom assessment tool for MPN patients participating in clinical trials globally. Disclosures: Vannucchi: Novartis: Consultancy. Samuelsson:Roche Sweden:. Harrison:Incyte: Honoraria; Novartis: Honoraria. Mesa:SBio: Research Funding; Novartis: Research Funding; Celgene: Research Funding; Incyte: Research Funding; Roche: Research Funding; eisai: Research Funding; telik: Research Funding.


2015 ◽  
Vol 22 (2) ◽  
pp. 223-224
Author(s):  
Kazi Monisur Rahman ◽  
Mst Habiba Khatun ◽  
Nasreen Fatema

The most common cause of hydatid disease in humans is infestation by the parasite Echinococcus granulousus. A 33 years old female patient with complaints of upper abdominal pain, discomfort, anorexia, nausea and loss of weight, was referred for ultrasound assessment of the whole of the abdomen. On ultrasound, her liver was enlarged in size. A fairly large cystic area measuring about (12 cm x 7.6 cm) having internal septations giving the appearance of cartwheel is noted in right lobe of liver. Intrahepatic biliary Channels and CBD were not dilated. Gall bladder, pancreas, spleen, both kidneys and other organs were found to be normal. No free fluid was seen in cul-de-sac. The patient was diagnosed as a case of echinococcosis in liver. DOI: http://dx.doi.org/10.3329/jdmc.v22i2.21548 J Dhaka Medical College, Vol. 22, No.2, October, 2013, Page 223-224


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