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Case 3
15y/boy presented with on and off
abdominal pain of 6months and a mass
felt to the left of umbilicus. USG FNA of
the mass done.
1. GCT
2. GCT with Embryonal Carcinoma
3. GCT/ALCL
4. Testicular GCT
5. Pleomorphic Adenocarcinoma-Pancreas
6. HCC
7. High Grade Malignant Tumour
8. ALCL, GCT
Review smears - Poorly differentiated
tumour
Adv. Repeat test at KMIO
Poorly differentiated tumour - ?GCT,
?ALCL
Case will be reviewed after workup
H’gram – Nml
Biochemistry – Nml LDH – 1674 ( 450-N)
Tumour markers – AFP, β-HCG – within Nml
HBsAg & HIV – Non-reactive
USG Abdomen – Enlarged multiple abdominal
mesenteric lymphnodes, largest 3x4x2.5cm
(FNA node) with mild splenomegaly.
Scrotal scan – NAD
No peripheral Lymphadenopathy
Advised IHC on cell block
Lymphnode Biopsy done
LCA
CD3 CD20
CD30
ALK+
PAX5 CD34
CD138
MUM1
Kappa Lamda
Ki67
EMA
CD4
A young boy,
Abdnominal lymphnodes++,
Non- immunocompramised,
H&E- high grade lesion.
IHC
LCA+ CD20-
CD3- CD30-
EMA+ CD34-
CK- CD4 +
ALK+(Granular) LMP1-
CD68- LMP1 ?
CD138- MUM1+
Kappa+ Lamda-
Ki67-65% Pax5 focal+
DIAGNOSIS
FINAL DIAGNOSIS
ALK Positive Diffuse Large B- Cell Lymphoma
ALK Positive Diffuse Large
• B- Cell Lymphoma
•1997 – Delsol workers – Delsol’s Tumour
•Median Age – 36yrs. Paed. – 30%
•High Stage Nodal Disease.
•No Assoc. with immunosuppression
•Poor prognosis – 11months
MORPH: Immunoblastic/plasmablastic,
Sinusoidal infiltration,
Appear deceptively cohesive – D/D Ca
IHC: LCA + 75%, CD+ 3% (weak & focal)
CD79a+ 16%, EMA+ 100%,
CD30+ 6% (weak & focal)
IHC contd
ƛ/ƙ+ 90% (IgA), CD138+/-, CD4+ 64%,
CD57+ 40%, CK+ rare,
ALK+ usually granular cytoplasm
Cytg: t(2:17)(q23;q23) – Fusion of CLTC
(clathrin) gene with ALK gene
t(2:5)(q23;q35)(NPM:ALK) – Rare
EBV – Neg.
NEOPLASIA
ALK-positive diffuse large B-cell lymphoma is
associated with Clathrin-ALK rearrangements:
report of 6 cases
Randy D. Gascoyne, Laurence Lamant, Jose I. Martin-Subero,
Valia S. Lestou, Nancy Lee Harris, Hans-Konrad Mu¨ ller-Hermelink,
John F. Seymour, Lynda J. Campbell, Douglas E. Horsman,
Isabelle Auvigne, Estelle Espinos, Reiner Siebert, and Georges Delsol
Blood. 2003;102:2568-2573
American Journal Clinical Pathology
(2011) Clinical Pathology, 136, 183-194.
Plasmablastic Lymphoma and
Related Disorders
Eric D. Hsi, MD1, Robert B. Lorsbach, MD, PhD2,
Falko Fend, MD3 and Ahmet Dogan, MD, PhD4
+Author Affiliations
1From the Department of Clinical Pathology, Cleveland Clinic, Cleveland, OH;
Department of Pathology, University of Arkansas for Medical Sciences, Little
Rock; 3Institute of Pathology, University Hospital Tuebingen, Eberhard-Karls
University, Tuebingen, Germany and 4Department of Laboratory Medicine a
and Pathology, Mayo Clinic, Rochester, MN
Case 3

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Case 3

  • 1. Case 3 15y/boy presented with on and off abdominal pain of 6months and a mass felt to the left of umbilicus. USG FNA of the mass done.
  • 2.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11. 1. GCT 2. GCT with Embryonal Carcinoma 3. GCT/ALCL 4. Testicular GCT 5. Pleomorphic Adenocarcinoma-Pancreas 6. HCC 7. High Grade Malignant Tumour 8. ALCL, GCT
  • 12.
  • 13.
  • 14. Review smears - Poorly differentiated tumour Adv. Repeat test at KMIO Poorly differentiated tumour - ?GCT, ?ALCL Case will be reviewed after workup
  • 15. H’gram – Nml Biochemistry – Nml LDH – 1674 ( 450-N) Tumour markers – AFP, β-HCG – within Nml HBsAg & HIV – Non-reactive USG Abdomen – Enlarged multiple abdominal mesenteric lymphnodes, largest 3x4x2.5cm (FNA node) with mild splenomegaly. Scrotal scan – NAD No peripheral Lymphadenopathy Advised IHC on cell block Lymphnode Biopsy done
  • 16.
  • 17.
  • 18. LCA
  • 20. ALK+
  • 22. MUM1
  • 24. EMA
  • 25. CD4
  • 26. A young boy, Abdnominal lymphnodes++, Non- immunocompramised, H&E- high grade lesion.
  • 27. IHC LCA+ CD20- CD3- CD30- EMA+ CD34- CK- CD4 + ALK+(Granular) LMP1- CD68- LMP1 ? CD138- MUM1+ Kappa+ Lamda- Ki67-65% Pax5 focal+
  • 29. FINAL DIAGNOSIS ALK Positive Diffuse Large B- Cell Lymphoma
  • 30. ALK Positive Diffuse Large • B- Cell Lymphoma •1997 – Delsol workers – Delsol’s Tumour •Median Age – 36yrs. Paed. – 30% •High Stage Nodal Disease. •No Assoc. with immunosuppression •Poor prognosis – 11months
  • 31. MORPH: Immunoblastic/plasmablastic, Sinusoidal infiltration, Appear deceptively cohesive – D/D Ca IHC: LCA + 75%, CD+ 3% (weak & focal) CD79a+ 16%, EMA+ 100%, CD30+ 6% (weak & focal)
  • 32. IHC contd ƛ/ƙ+ 90% (IgA), CD138+/-, CD4+ 64%, CD57+ 40%, CK+ rare, ALK+ usually granular cytoplasm Cytg: t(2:17)(q23;q23) – Fusion of CLTC (clathrin) gene with ALK gene t(2:5)(q23;q35)(NPM:ALK) – Rare EBV – Neg.
  • 33. NEOPLASIA ALK-positive diffuse large B-cell lymphoma is associated with Clathrin-ALK rearrangements: report of 6 cases Randy D. Gascoyne, Laurence Lamant, Jose I. Martin-Subero, Valia S. Lestou, Nancy Lee Harris, Hans-Konrad Mu¨ ller-Hermelink, John F. Seymour, Lynda J. Campbell, Douglas E. Horsman, Isabelle Auvigne, Estelle Espinos, Reiner Siebert, and Georges Delsol Blood. 2003;102:2568-2573
  • 34. American Journal Clinical Pathology (2011) Clinical Pathology, 136, 183-194. Plasmablastic Lymphoma and Related Disorders Eric D. Hsi, MD1, Robert B. Lorsbach, MD, PhD2, Falko Fend, MD3 and Ahmet Dogan, MD, PhD4 +Author Affiliations 1From the Department of Clinical Pathology, Cleveland Clinic, Cleveland, OH; Department of Pathology, University of Arkansas for Medical Sciences, Little Rock; 3Institute of Pathology, University Hospital Tuebingen, Eberhard-Karls University, Tuebingen, Germany and 4Department of Laboratory Medicine a and Pathology, Mayo Clinic, Rochester, MN