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Case Presentation

A 71-year-old man presented with dysphagia, weight loss, and nausea. Endoscopy revealed an esophageal stricture. Biopsy of the esophagus showed Hodgkin lymphoma of the mixed cellularity subtype. Immunohistochemistry was positive for CD15 and CD30. The diagnosis was isolated esophageal Hodgkin lymphoma.

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Genio Aladdin
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0% found this document useful (0 votes)
47 views

Case Presentation

A 71-year-old man presented with dysphagia, weight loss, and nausea. Endoscopy revealed an esophageal stricture. Biopsy of the esophagus showed Hodgkin lymphoma of the mixed cellularity subtype. Immunohistochemistry was positive for CD15 and CD30. The diagnosis was isolated esophageal Hodgkin lymphoma.

Uploaded by

Genio Aladdin
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Case Presentation
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Presented by : Adham Alaa El-Din,


Pathology TA at Badr University
Supervised by: Prof. Dr. Marwa Mosaad
Faculty of Medicine, Ain Shams Univesity
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History
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• A •71-year-old
Third levelgentleman presented with a 6-month history of
progressive dysphagia,
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weight loss and nausea.
• Examination revealed
• Fifth level a cachexic, frail gentleman who had clear
dysphagia to solids and liquids.
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Findings
• His initial blood investigations revealed a Hb of 125 g/L, WCC 3.6
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x10 9 text styles
/L (neutrophils 2.14, lymphocytes 1.03, eosinophils 0.07), Plt
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x109/L.
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• Urea level
and electrolytes, liver function tests, albumin, calcium and
phosphate were level
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mm and c-reactive protein was 43 mg/dL.
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• Given the suspicion of gastro-intestinal pathology he underwent an
upper gastro-intestinal endoscopy, which revealed a stricture at 25
cm.
• A staging CT of chest and abdomen was performed revealing a
generally thickened oesophagus, with no significant
lymphadenopathy in the chest or abdomen. The solid intra-
abdominal organs were unremarkable.
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Initial endoscopy (a), and repeat procedure with stent insertion (b).
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Microscopic
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examination
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Click What
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your diagnosis?
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Click to editDiagnosis
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Isolated oesophageal
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Hodgkin lymphoma
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Mixed cellularity subtype


IHC title style
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CD15
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diagnosis
Tumors characterised by dual population of
cells (small
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•T-cell–rich large B-cell lymphoma (TCRLBCL) variant of
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DLBCL •
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Follicular lymphoma

Anaplastic large cell lymphoma

Thymoma type B1
T-cell–rich large B-cell lymphoma (variant of
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DLBCL)to edit Master title style
• Edit Master infiltrate
• Diffuse text styleswithout sclerosis or nodularity
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• Scattered
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large, mononuclear neoplastic cells in
a background
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are almost• Fifthall T cells
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• Large neoplastic B-cells are positive for CD45


and CD20, negative for CD15 and CD30
• Background T-cells are positive for CD3 and
CD8
Hodgkin TCRLBCL
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CD20
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CD15
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CD30 CD3
Nodular Lymphocyte Predominance HL vs.
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large B-cell title style
lymphoma

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Differential title style
diagnosis
Tumors characterised by dual population of
cells (small
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T-cell–rich
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level B-cell lymphoma (TCRLBCL) variant of
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Follicular lymphoma

Anaplastic large cell lymphoma

Thymoma type B1
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• Patients text styles older than 40 years.
usually
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• Variable mixture of centrocytes and centroblasts
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without polymorphic
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• Reed-Sternberg–like cells rarely present; sclerosis is
incidental.
• Both small and large cells are CD20-positive B
cells; may express CD10 and usually express Bcl-2.
• Characteristic t(14;18) chromosomal translocation
(IGH on chromosome 14, Bcl-2 on chromosome 18)
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Hodgkin Follicular
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CD15 CD20
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CD30
BCl2
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diagnosis
Tumors characterised by dual population of
cells (small
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T-cell–rich
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level B-cell lymphoma (TCRLBCL) variant of
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Follicular lymphoma

Anaplastic large cell lymphoma

Thymoma type B1
Anaplastic
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• Large cells are usually predominant and often
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resemble largestyles
cell lymphoma or metastatic
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• carcinoma
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• Hallmark cells
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horseshoe-shaped
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• Abnormal large cells are positive for CD30; usually


T cells but may not express common T-cell antigens
or CD45
• Tumor cells are typically positive for EMA and
often anaplastic lymphoma kinase (ALK-1)
• Negative for CD15, PAX5, and fascin
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CD30
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Hodgkin ALCL
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CD15
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CD30 CD30
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H&E
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ALK
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diagnosis
Tumors characterised by dual population of
cells (small
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T-cell–rich
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level B-cell lymphoma (TCRLBCL) variant of
DLBCL • Fourth level
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Follicular lymphoma

Anaplastic large cell lymphoma

Thymoma type B1
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B1)title style
• Large
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• Few level scattered round or polygonal thymic
isolated,
epithelial cells with minimal cytologic atypia.
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• Medullary islands
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elements.
• Tumor cells are typically positive for pan-
cytokeratin.
• Reactive small T lymphocytes are positive for CD3.
• Thymocytes are positive for TdT.
• Negative for CD30, CD15.
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AE1/
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TdT
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Take-Home Messagetitle style
• Esophageal lymphoma is rare, accounting for less than 1%
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all gastrointestinal
text styleslymphomas.
•• The incidence
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intestinal lymphoma is about 1% and most cases are low
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grade B-cell mucosa associated lymphoid tissue (MALT
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lymphoma) or diffuse
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• No definite specific aetiological factors and oesophageal
infections have been identified as predisposing factors,
although there remains an increased risk of lymphoma in
patients with immunodeficiency.
• Surgery has a limited place in the treatment of primary
oesophageal lymphoma. The standard treatment is tailored
to the stage and usually includes a combination of chemo
and radiotherapy.
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