Cargando…

A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma

BACKGROUND: Although secondary liver involvement of the lymphoma is common and occurs in 50% of patients with non-Hodgkin’s lymphoma, liver tumor rupture in malignant lymphoma is extremely rare. We report a case of a spontaneously ruptured secondary liver involvement of non-Hodgkin’s lymphoma that w...

Descripción completa

Detalles Bibliográficos
Autores principales: Oshita, Ko, Itamoto, Toshiyuki, Oshita, Akihiko, Nakahara, Hideki, Nishisaka, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934290/
https://www.ncbi.nlm.nih.gov/pubmed/29725882
http://dx.doi.org/10.1186/s40792-018-0451-2
_version_ 1783320091329298432
author Oshita, Ko
Itamoto, Toshiyuki
Oshita, Akihiko
Nakahara, Hideki
Nishisaka, Takashi
author_facet Oshita, Ko
Itamoto, Toshiyuki
Oshita, Akihiko
Nakahara, Hideki
Nishisaka, Takashi
author_sort Oshita, Ko
collection PubMed
description BACKGROUND: Although secondary liver involvement of the lymphoma is common and occurs in 50% of patients with non-Hodgkin’s lymphoma, liver tumor rupture in malignant lymphoma is extremely rare. We report a case of a spontaneously ruptured secondary liver involvement of non-Hodgkin’s lymphoma that was successfully treated with transcatheter arterial embolization (TAE) to obtain hemostasis, and subsequent hepatectomy and systemic chemotherapy. To the best of our knowledge, this is only the second reported case of a ruptured hepatic lymphoma. CASE PRESENTATION: A 74-year-old man with sudden-onset right shoulder and upper quadrant pain was transferred to our hospital via an ambulance. His vital signs were stable. Contrast-enhanced computed tomography showed a large hypo-enhancing tumor (94 × 81 mm) in the posterior segment of the liver, with intratumoral extravasation and a 12 × 10 mm daughter tumor in segment 5 of the liver. Hemoperitoneum due to rupture of hepatocellular carcinoma with intratumoral hemorrhage was suspected, although the serum alpha-fetoprotein and protein induced by vitamin K absence-II levels were within normal range. TAE was used for hemostasis. Extended posterior segmentectomy including tumor resection in segment 5 was performed on day 23 after embolization. The postoperative course was uneventful. Pathological examination of the resected specimens revealed that the ruptured tumor was diffuse large B-cell lymphoma. Postoperative fluorodeoxyglucose positron emission tomography-computed tomography showed uptake in the left parotid gland, pancreas, and thoracic vertebra. Based on these findings, the final diagnosis was a ruptured secondary hepatic malignant lymphoma. Complete remission was achieved with chemotherapy. He remains alive 30 months after hepatectomy without evidence of relapse. CONCLUSIONS: We report the first case describing a hepatic tumor rupture as the first presentation of a primary or secondary hepatic malignant lymphoma. The patient was successfully treated with TAE, hepatectomy, and subsequent systemic chemotherapy for non-Hodgkin’s lymphoma.
format Online
Article
Text
id pubmed-5934290
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-59342902018-05-09 A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma Oshita, Ko Itamoto, Toshiyuki Oshita, Akihiko Nakahara, Hideki Nishisaka, Takashi Surg Case Rep Case Report BACKGROUND: Although secondary liver involvement of the lymphoma is common and occurs in 50% of patients with non-Hodgkin’s lymphoma, liver tumor rupture in malignant lymphoma is extremely rare. We report a case of a spontaneously ruptured secondary liver involvement of non-Hodgkin’s lymphoma that was successfully treated with transcatheter arterial embolization (TAE) to obtain hemostasis, and subsequent hepatectomy and systemic chemotherapy. To the best of our knowledge, this is only the second reported case of a ruptured hepatic lymphoma. CASE PRESENTATION: A 74-year-old man with sudden-onset right shoulder and upper quadrant pain was transferred to our hospital via an ambulance. His vital signs were stable. Contrast-enhanced computed tomography showed a large hypo-enhancing tumor (94 × 81 mm) in the posterior segment of the liver, with intratumoral extravasation and a 12 × 10 mm daughter tumor in segment 5 of the liver. Hemoperitoneum due to rupture of hepatocellular carcinoma with intratumoral hemorrhage was suspected, although the serum alpha-fetoprotein and protein induced by vitamin K absence-II levels were within normal range. TAE was used for hemostasis. Extended posterior segmentectomy including tumor resection in segment 5 was performed on day 23 after embolization. The postoperative course was uneventful. Pathological examination of the resected specimens revealed that the ruptured tumor was diffuse large B-cell lymphoma. Postoperative fluorodeoxyglucose positron emission tomography-computed tomography showed uptake in the left parotid gland, pancreas, and thoracic vertebra. Based on these findings, the final diagnosis was a ruptured secondary hepatic malignant lymphoma. Complete remission was achieved with chemotherapy. He remains alive 30 months after hepatectomy without evidence of relapse. CONCLUSIONS: We report the first case describing a hepatic tumor rupture as the first presentation of a primary or secondary hepatic malignant lymphoma. The patient was successfully treated with TAE, hepatectomy, and subsequent systemic chemotherapy for non-Hodgkin’s lymphoma. Springer Berlin Heidelberg 2018-05-03 /pmc/articles/PMC5934290/ /pubmed/29725882 http://dx.doi.org/10.1186/s40792-018-0451-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Case Report
Oshita, Ko
Itamoto, Toshiyuki
Oshita, Akihiko
Nakahara, Hideki
Nishisaka, Takashi
A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma
title A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma
title_full A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma
title_fullStr A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma
title_full_unstemmed A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma
title_short A rare case of a spontaneously ruptured secondary hepatic malignant lymphoma
title_sort rare case of a spontaneously ruptured secondary hepatic malignant lymphoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934290/
https://www.ncbi.nlm.nih.gov/pubmed/29725882
http://dx.doi.org/10.1186/s40792-018-0451-2
work_keys_str_mv AT oshitako ararecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT itamototoshiyuki ararecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT oshitaakihiko ararecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT nakaharahideki ararecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT nishisakatakashi ararecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT oshitako rarecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT itamototoshiyuki rarecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT oshitaakihiko rarecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT nakaharahideki rarecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma
AT nishisakatakashi rarecaseofaspontaneouslyrupturedsecondaryhepaticmalignantlymphoma