Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literature

Hodgkin lymphoma (HL) is mainly considered a nodal disease but extra nodal involvement can also be seen with variable frequency. Solitary bone involvement in HL known as Primary osseous hodgkin lymphoma (POHL) is very rare. It is defined as a lymphoma that is restricted to the bone without any simul...

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Main Authors: Durr-e- Amna Siddiqui, Hira Feroz Akbar, Hassan Sadiq, Namirah Iftikhar, Muhammad Rahil Khan, Muhammad Rafie Raza
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Cancer Treatment and Research Communications
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2468294221001453
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author Durr-e- Amna Siddiqui
Hira Feroz Akbar
Hassan Sadiq
Namirah Iftikhar
Muhammad Rahil Khan
Muhammad Rafie Raza
author_facet Durr-e- Amna Siddiqui
Hira Feroz Akbar
Hassan Sadiq
Namirah Iftikhar
Muhammad Rahil Khan
Muhammad Rafie Raza
author_sort Durr-e- Amna Siddiqui
collection DOAJ
description Hodgkin lymphoma (HL) is mainly considered a nodal disease but extra nodal involvement can also be seen with variable frequency. Solitary bone involvement in HL known as Primary osseous hodgkin lymphoma (POHL) is very rare. It is defined as a lymphoma that is restricted to the bone without any simultaneous organ or lymph node involvement at the time of initial diagnosis. Primary Hodgkin lymphoma of the bone can be very challenging to diagnose because of its rarity especially in children and its variable presentation. Here we report the youngest case of POHL in a girl 7 years of age. She presented with the left leg pain and B-symptoms of fever and weight loss. Initial workup and imaging were suggestive of infection or a bone tumor. Bone biopsy of left hip joint after the multiple courses of antibiotics revealed Reed Sternberg cells in the mixed inflammatory background with CD30 and PAX-5 immunohistochemical positivity confirming classical hodgkin lymphoma, mixed cellularity type. CD99 and CD1a were negative excluding ewing sarcoma and langerhan cell Histiocytosis respectively. Absence of significant lymphadenopathy or visceromegaly on staging computerized tomography (CT) scan confirmed a very rare POHL. She received standard conventional chemotherapy with radiation. Our patient is in remission for five years after treatment.
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spelling doaj.art-74b261844c5844c08e28e2ce2fdafe542022-12-21T19:35:26ZengElsevierCancer Treatment and Research Communications2468-29422021-01-0129100448Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literatureDurr-e- Amna Siddiqui0Hira Feroz Akbar1Hassan Sadiq2Namirah Iftikhar3Muhammad Rahil Khan4Muhammad Rafie Raza5Dow University of Health Science, Karachi, PakistanDow University of Health Science, Karachi, Pakistan; Corresponding author.Dow University of Health Science, Karachi, PakistanDow University of Health Science, Karachi, PakistanPediatric Hamatology Oncology, The Indus Hospital, Karachi, PakistanPediatric Hamatology Oncology, The Indus Hospital, Karachi, PakistanHodgkin lymphoma (HL) is mainly considered a nodal disease but extra nodal involvement can also be seen with variable frequency. Solitary bone involvement in HL known as Primary osseous hodgkin lymphoma (POHL) is very rare. It is defined as a lymphoma that is restricted to the bone without any simultaneous organ or lymph node involvement at the time of initial diagnosis. Primary Hodgkin lymphoma of the bone can be very challenging to diagnose because of its rarity especially in children and its variable presentation. Here we report the youngest case of POHL in a girl 7 years of age. She presented with the left leg pain and B-symptoms of fever and weight loss. Initial workup and imaging were suggestive of infection or a bone tumor. Bone biopsy of left hip joint after the multiple courses of antibiotics revealed Reed Sternberg cells in the mixed inflammatory background with CD30 and PAX-5 immunohistochemical positivity confirming classical hodgkin lymphoma, mixed cellularity type. CD99 and CD1a were negative excluding ewing sarcoma and langerhan cell Histiocytosis respectively. Absence of significant lymphadenopathy or visceromegaly on staging computerized tomography (CT) scan confirmed a very rare POHL. She received standard conventional chemotherapy with radiation. Our patient is in remission for five years after treatment.http://www.sciencedirect.com/science/article/pii/S2468294221001453Hodgkin lymphoma of bonePrimary osseous hodgkin lymphomaPOHLBone tumorYoungest child
spellingShingle Durr-e- Amna Siddiqui
Hira Feroz Akbar
Hassan Sadiq
Namirah Iftikhar
Muhammad Rahil Khan
Muhammad Rafie Raza
Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literature
Cancer Treatment and Research Communications
Hodgkin lymphoma of bone
Primary osseous hodgkin lymphoma
POHL
Bone tumor
Youngest child
title Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literature
title_full Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literature
title_fullStr Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literature
title_full_unstemmed Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literature
title_short Primary Hodgkin's Lymphoma of bone in 7-year-old- an exceptional case report of youngest child in literature
title_sort primary hodgkin s lymphoma of bone in 7 year old an exceptional case report of youngest child in literature
topic Hodgkin lymphoma of bone
Primary osseous hodgkin lymphoma
POHL
Bone tumor
Youngest child
url http://www.sciencedirect.com/science/article/pii/S2468294221001453
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