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SSR Inst. Int. J. Life Sci.
Singh et al., 2019
DOI:10.21276/SSR-IIJLS.2019.5.1.12
Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2196
Primary Mucinous Adenocarcinoma of Gall Bladder: A Rare Case
Report
Mahendra Singh1
, Anveksha Sachan2*
, Anita Omhare3
, Neelima Verma4
, Swetlana Sachan5
1
Professor and Head, Department of Pathology, GSVM Medical College Kanpur, India
2
Junior Resident, Department of Pathology, GSVM Medical College Kanpur, India
3
Lecturer, Department of Pathology, GSVM Medical College Kanpur, India
4
Associate Professor, Department of Pathology, GSVM Medical College Kanpur, India
5
Junior Resident, Department of Pathology, GSVM Medical College Kanpur, India
*Address for Correspondence: Dr. Anveksha Sachan, Junior Resident, Department of Pathology, GSVM Medical
College, Kanpur, Uttar Pradesh, India
E-mail: riyasachan12@gmail.com
Received: 21 Aug 2018/ Revised: 27 Oct 2018/ Accepted: 23 Dec 2018
ABSTRACT
Background: Mucinous carcinoma of the gall bladder is a rare variant of gall bladder carcinoma. Mucinous carcinoma of gall
bladder is characterized by extracellular mucin comprising of >50% of tumor volume.
Methods: We reported a case of 50 years old female with chief complaints of pain in right hypochondriac region, vomiting, weight
loss, loss of appetite and indigestion. Her liver function test was deranged. Ultrasonography revealed markedly distended gall
bladder with thickened and edematous wall and lumen was filled with multiple calculi. Contrast enhanced Computed Tomography
(CECT) revealed multiple enlarged lymph nodes. Carbohydrate antigen (CA) 19.9 cancer marker was found within normal limit. The
diagnosis was confirmed by histopathological examination of cholecystectomy specimen.
Results: Patient presents with pain in right hypochondriac region, weight loss, loss of appetite and on histopathological
examination of gall bladder, findings were suggestive of primary mucinous adenocarcinoma of gall bladder.
Conclusion: Mucinous adenocarcinoma was a rare variant of gall bladder carcinoma. It had more aggressive behavior and worse
prognosis than that of conventional adenocarcinoma of Gall Bladder.
Key-words: Cholecystectomy, Gall bladder, Hypochondriac, Mucinous adenocarcinoma, Mucin
INTRODUCTION
Mucinous Carcinoma of gall bladder is a rare variant of
gall bladder carcinoma, constitutes 2.5% of gallbladder
carcinomas. Mucinous carcinoma of gallbladder is
characterized by extracellular mucin comprising > 50% of
tumor volume [1]
. When mucinous component exceeds
90% of the tumour is labeled as pure mucinous
carcinoma [2-4]
. We reported a case of mucinous
adenocarcinoma of gallbladder. Mucinous cell carcinoma
is a very uncommon neoplasm of gallbladder, most of
them displaying a mixed-mucinous histological picture.
How to cite this article
Singh M, Sachan A, Omhare A, Verma N, Sachan S Primary
Mucinous Adenocarcinoma of Gall Bladder: A Rare Case Report.
SSR Inst. Int. J. Life Sci., 2019; 5(1): 2196-2200.
Access this article online
https://iijls.com/
Most carcinomas arise in the fund us (60%), body (30%)
and neck (10%) [5]
. Tumor has a poor prognosis because
of its tendency toward invasive growth [5]
. Approximately
3:1 ratio between female: male occur and most patients
are older than 50 years [6]
. Carcinomas with copious
mucin production are now thought to form distinct
category among malignancies of gall bladder [6]
. It’s
incidence increases with age [6]
. Risk factor for gall
bladder carcinoma is well known but a definite
epidemiologic parallel between gall bladder carcinoma
and cholelithiasis occur [6]
.
MATERIALS AND METHODS
Cholecystectomy specimen and the hysterectomy
specimen of the same patient were sent for
histopathological examination in our Department of
Pathology, GSVM Medical College, Kanpur, India from a
private hospital in the year of 2018. Both the specimens
Case Report
SSR Inst. Int. J. Life Sci.
Singh et al., 2019
DOI:10.21276/SSR-IIJLS.2019.5.1.12
Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2197
were fixed in 10% buffered formalin for 24-48 hours.
After that the tissues were processed and stained by
hematoxylin and eosin staining and then mounted with
DPX.
CASE REPORT
A 50 years old female was presented with complaints of
pain in the right hypochondriac region, vomiting, and
weight loss since 45 days along with the history of loss of
appetite and indigestion for 20 days.
On examination, her vital parameters were within
normal limits. Renal function test was within the normal
limit. Hematological parameters revealed mildly raised.
TLC was found, the 13,300 cells/mm3
. Biochemical
investigation (liver function test) was shown deranged
parameters in Table 1.
Table 1: Liver function test
Biochemical
parameters
Obtained
value
Normal reference
Range
S. Bilirubin Total
Direct
Indirect
13.1 mg/dl
2.0 mg/dl
11.1 mg/dl
0.3 – 1.0 mg/dl
0.0 to 0.2 mg/dl
0.4 to 0.8 mg/dl
S.G.P.T. 108 U/L 5 – 42 U/L
S.G.O.T. 130 U/L 5 – 40 U/L
S. Alkaline
phosphatase
1485 U/L 25 - 120 U/L
USG findings of the patient revealed markedly distended
gall bladder with thickened and edematous gallbladder
wall and lumen was filled with multiple calculi. The
proximal part of common bile duct not adequately
visualized due to theedematous gallbladder wall. A Liver
was mildly enlarged with intra-hepatic biliary channels
slightly dilated. One month after cholecystectomy, CECT
whole abdomen was performed which revealed multiple
lymph nodes in peri-portal, peri-pancreatic, coeliac,
pre-aortic, para-aortic, aorto-caval lymph nodes up to
1.5 cm- Lymph nodal secondaries. Also, there were mild
as cites with mild hepatosplenomegaly.
* CA 19.9 cancer marker was also done, which was found
within normal limit.
Gross- Cholecystectomy and hysterectomy specimen of
the same patient were sent to the Pathology department
of GSVM Medical College, Kanpur, in two separate jars
for histopathological examination.
JAR I was labeled gall bladder as Cholecystectomy
specimen measured 8x4 and 5x2 cm. The outer surface
showed few fibro fatty adhesions. On cut section, inner
surface showed glistening mucosa with a greyish white
area. Wall thickness varies from 1.5 to 2 cm. There were
multiple stones inside the jar shown in Fig. 1 (A,B).
Fig. 1 (A): Cholecystectomy specimen shows a greyish
white area
Fig. 1 (B): Cholecystectomy specimen shows a glistening
mucosa on cut section
JAR II was labeled total abdominal hysterectomy. The
specimen consisted of the uterus, cervix with bilateral
adnexa.
Microscopy examination- Multiple H & E stained
sections from gall bladder were examined shows marked
thickening of gallbladder wall comprising of mucosa,
muscular layer and serosa.
B
A
SSR Inst. Int. J. Life Sci.
Singh et al., 2019
DOI:10.21276/SSR-IIJLS.2019.5.1.12
Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2198
Numerous well-demarcated mucin pools with atypical
cells (floating into the mucin pools) having a high
nucleocytoplasmic ratio, moderate amount of
vacuolated cytoplasm, were seen on the mucosal surface
(Fig. 2 to Fig. 5).
These mucin pools were surrounded by inflammatory
cells infiltrate comprising of mature lymphocytes,
macrophages and fibroblasts along with few congested
and dilated blood vessels. These atypical cells and mucin
pools were also in filtrating the muscle layer with similar
picture and were also involving up to the serosa. Findings
were suggestive of primary mucinous adenocarcinoma of
gallbladder. Microscopic findings of received
hysterectomy specimen were histopathologically normal.
DISCUSSION
Gallbladder carcinoma is the fifth most common G. I.
malignancy [7]
. It is a disease of elderly, more common in
females than in males (3:1) and there are various types
of gall bladder carcinoma such as adenocarcinoma,
squamous cell carcinoma, adenosquamous carcinoma
and very rare mucinous adenocarcinoma [5]
.
Mucinous carcinoma has two histologic variants. One
with large pool of extracellular mucin with groups of
tumour cells and other types with cystically dilated
mucin filled glands. These may be present either alone or
in combination [1]
.
In the majority of cases mucinous adenocarcinoma was
frequently well-differentiated and admixed with
conventional adenocarcinoma but poorly differentiated
mucinous adenocarcinoma with distant metastasis can
be found. Focal mucinous differentiation and well-
differentiated adenocarcinoma with intra glandular
mucin also occur [8]
. Mucinous carcinoma constitutes
only 2.5%. This was rather uncommon in gall bladder and
is noted in the literature mostly as individual case
reports or small handful of cases [6]
.
Presence of gall stones is one of the major risk factors for
gallbladder adenocarcinoma, as in our case report but
Fig. 2: Scanner view (4x) shows well-demarcated mucin
pools
Fig. 3: Low power view (10x) shows mucin pool
surrounded by inflammatory cells infiltrate and few
blood vessels
Fig. 4: Low power view (10x) shows an involvement of
serosa
Fig. 5: High power view (40x) shows clusters of
neoplastic cells floating in mucin
SSR Inst. Int. J. Life Sci.
Singh et al., 2019
DOI:10.21276/SSR-IIJLS.2019.5.1.12
Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2199
10-25% of patients with gall bladder carcinoma. They do
not have associated cholelithiasis [9]
. We can differentiate
mucinous carcinoma from conventional gall bladder
adenocarcinoma by MUC 2 positivity and from intestinal
carcinoma by inverse CK7/CK20 profiles [10]
CK7 (+) and
CK20 (-) [11]
.
It was CDX2 (Negative) so can be differentiated from
pancreatic mucinous carcinoma [12]
. It was MUC6
(Negative) so can be differentiated from mammary
colloid carcinoma [13]
. Owing to the location of
gallbladder, dissemination of tumor to adjacent tissue is
usually present at the time of diagnosis. Most patients
were not suitable for curative surgery because of
advanced stage of the disease [7]
.
CONCLUSIONS
Mucinous adenocarcinoma is a rare variant of gall
bladder carcinoma. It has more aggressive behavior and
worse prognosis than that of conventional
adenocarcinoma of gall bladder. Most mucinous
carcinoma is a mixed-mucinous, not pure colloid type. It
is very essential to differentiate a primary mucinous
adenocarcinoma from metastatic mucinous
adenocarcinoma arising from other sites/organs because
of different modes of treatment and different prognosis.
Tumour markers have increasing significance in the
diagnosis and evaluation of gall bladder carcinoma. Assay
of carbohydrate antigen (CA) 242, carbohydrate antigen
(CA) 15-3, carbohydrate antigen (CA) 19-9 and
carbohydrate antigen (CA) 125 were fairly good markers
for discriminating patients of carcinoma of the gall
bladder from cholelithiasis. CA242 and CA125, when
used together achieved best sensitivity and specificity.
Serum markers seem to be less sensitive when used
individually in carcinoma of the gall bladder but may
prove useful in combination.
ACKNOWLEDGMENTS
The authors are highly grateful to the respective
Universities and Principals of relevant Institutions to
carry out the present investigations.
CONTRIBUTION OF AUTHORS
Research concept- Dr. Anveksha Sachan
Research design- Dr. Neelima Verma
Supervision- Dr. Anita Omhare
Materials- Dr. Anita Omhare
Data collection- Dr. Anita Omhare
Data analysis and interpretation- Dr. Anita Omhare
Literature search- Dr. Swetlana Sachan
Writing article- Dr. Anveksha Sachan
Critical review- Dr. Mahendra Singh
Article editing- Dr. Anveksha Sachan
Final approval- Dr. Anveksha Sachan
REFERENCES
[1] Albores SJ, Menck HR, Scoazec JC, Soehendra N,
Wittekind C, Sriram PV, et al. Carcinoma of the
gallbladder and extra hepatic bile ducts. In: Hamilton
SR, Aaltonen LA, editors. WHO Classification of
Tumors. Pathology and Genetics of Tumors of the
Digestive system. Lyon: IARC Press, 2000; pp. 206-12.
[2] Adsay VN, Klimstra DS. Benign and malignant Tumors
of gall bladder and extra hepatic biliary tract. In:
Odze RD, Goldblum JR, editors. Surgical pathology of
the GI tract, liver, biliary tract and pancreas. 2nd
ed.
Philadelphia: Saunders Elsevier 2009; pp. 857-70.
[3] Adsay VN. Gall Bladder, Extra hepatic biliary Tree,
and Ampulla. In: Mills SE, editor. Sternberg’s
Diagnostic surgical pathology. 5th
ed. Lippincott
Williams and Wilkins, 2010; pp. 1620-24.
[4] [1] Gupte PA, Chaturvedi R, Patil LY, Joshi AS. Pure
mucinous (Colloid) adenocarcinoma of the Gall
bladder– A rare phenotype. Oncol. Gastroenterol.
Hepatol. Reports, 2013; 2(1): 27-29.
[5] Misra S, Chaturvedi A, Misra NC, Sharma ID.
Carcinoma of gall bladder. Lancet oncol., 2003; 4(3):
167-76.
[6] Tangde AR, Rathod SG, Joshi AR, Bindu RS. Mucinous
adenocarcinoma of gall bladder: A case report. Int. J.
Res. Med. Sci., 2017; 5(11): 5082–84.
[7] Abd-Allah MA, Ali MHM, Khalid OI, Gazali M, Dr M.
Allata AA. Mucinous Adenocarcinoma of the
Gallbladder: A Case Report. Int. J. Multidisciplinary
Curr. Res., 2016; 4: 37-38.
[8] Singh M, Vishwakarma I, Purwar N, Verma YN,
Sharma T. Mucinous carcinoma of Gall Bladder an
incidental Finding of a rare case. Int. J. Life Sci.
Scient. Res., 2017; 3(5): 1411-14.
[9] Dursun N, Escalona OT, Roa JC, Basturk O, Bagci P, et
al. Mucinous carcinoma of Gall bladder:
Clinicopathologic analysis of 15 cases identified in
606 carcinomas. Arch. Pathol. Lab. Med., 2012;
136(1): 1347-58.
SSR Inst. Int. J. Life Sci.
Singh et al., 2019
DOI:10.21276/SSR-IIJLS.2019.5.1.12
Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2200
[10]Allah AAM, Ali MHM, et al. Mucinous Adeno
carcinoma of gall bladder: A case report. Int. J.
multidisciplinary Curr. Res., 2016; 4: 37–38.
[11]Mills SE, Greenson JK, et al. Surgical histopathology
Sternberg’s 6th
edition; 2015; 1797-1802.
[12]Miller SE, Greenson JK, et al. Surgical histopathology
Sternberg’s 6th
Ed: 2015, pp. 1617.
[13]Rosai J. Ackerman’s surgical pathology Rosai &
Ackerman’s. 10th
Ed: 2012, pp. 1700.
Open Access Policy:
Authors/Contributors are responsible for originality, contents, correct references, and ethical issues. SSR-IIJLS publishes all articles under Creative
Commons Attribution- Non-Commercial 4.0 International License (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/legalcode

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  • 1. SSR Inst. Int. J. Life Sci. Singh et al., 2019 DOI:10.21276/SSR-IIJLS.2019.5.1.12 Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2196 Primary Mucinous Adenocarcinoma of Gall Bladder: A Rare Case Report Mahendra Singh1 , Anveksha Sachan2* , Anita Omhare3 , Neelima Verma4 , Swetlana Sachan5 1 Professor and Head, Department of Pathology, GSVM Medical College Kanpur, India 2 Junior Resident, Department of Pathology, GSVM Medical College Kanpur, India 3 Lecturer, Department of Pathology, GSVM Medical College Kanpur, India 4 Associate Professor, Department of Pathology, GSVM Medical College Kanpur, India 5 Junior Resident, Department of Pathology, GSVM Medical College Kanpur, India *Address for Correspondence: Dr. Anveksha Sachan, Junior Resident, Department of Pathology, GSVM Medical College, Kanpur, Uttar Pradesh, India E-mail: riyasachan12@gmail.com Received: 21 Aug 2018/ Revised: 27 Oct 2018/ Accepted: 23 Dec 2018 ABSTRACT Background: Mucinous carcinoma of the gall bladder is a rare variant of gall bladder carcinoma. Mucinous carcinoma of gall bladder is characterized by extracellular mucin comprising of >50% of tumor volume. Methods: We reported a case of 50 years old female with chief complaints of pain in right hypochondriac region, vomiting, weight loss, loss of appetite and indigestion. Her liver function test was deranged. Ultrasonography revealed markedly distended gall bladder with thickened and edematous wall and lumen was filled with multiple calculi. Contrast enhanced Computed Tomography (CECT) revealed multiple enlarged lymph nodes. Carbohydrate antigen (CA) 19.9 cancer marker was found within normal limit. The diagnosis was confirmed by histopathological examination of cholecystectomy specimen. Results: Patient presents with pain in right hypochondriac region, weight loss, loss of appetite and on histopathological examination of gall bladder, findings were suggestive of primary mucinous adenocarcinoma of gall bladder. Conclusion: Mucinous adenocarcinoma was a rare variant of gall bladder carcinoma. It had more aggressive behavior and worse prognosis than that of conventional adenocarcinoma of Gall Bladder. Key-words: Cholecystectomy, Gall bladder, Hypochondriac, Mucinous adenocarcinoma, Mucin INTRODUCTION Mucinous Carcinoma of gall bladder is a rare variant of gall bladder carcinoma, constitutes 2.5% of gallbladder carcinomas. Mucinous carcinoma of gallbladder is characterized by extracellular mucin comprising > 50% of tumor volume [1] . When mucinous component exceeds 90% of the tumour is labeled as pure mucinous carcinoma [2-4] . We reported a case of mucinous adenocarcinoma of gallbladder. Mucinous cell carcinoma is a very uncommon neoplasm of gallbladder, most of them displaying a mixed-mucinous histological picture. How to cite this article Singh M, Sachan A, Omhare A, Verma N, Sachan S Primary Mucinous Adenocarcinoma of Gall Bladder: A Rare Case Report. SSR Inst. Int. J. Life Sci., 2019; 5(1): 2196-2200. Access this article online https://iijls.com/ Most carcinomas arise in the fund us (60%), body (30%) and neck (10%) [5] . Tumor has a poor prognosis because of its tendency toward invasive growth [5] . Approximately 3:1 ratio between female: male occur and most patients are older than 50 years [6] . Carcinomas with copious mucin production are now thought to form distinct category among malignancies of gall bladder [6] . It’s incidence increases with age [6] . Risk factor for gall bladder carcinoma is well known but a definite epidemiologic parallel between gall bladder carcinoma and cholelithiasis occur [6] . MATERIALS AND METHODS Cholecystectomy specimen and the hysterectomy specimen of the same patient were sent for histopathological examination in our Department of Pathology, GSVM Medical College, Kanpur, India from a private hospital in the year of 2018. Both the specimens Case Report
  • 2. SSR Inst. Int. J. Life Sci. Singh et al., 2019 DOI:10.21276/SSR-IIJLS.2019.5.1.12 Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2197 were fixed in 10% buffered formalin for 24-48 hours. After that the tissues were processed and stained by hematoxylin and eosin staining and then mounted with DPX. CASE REPORT A 50 years old female was presented with complaints of pain in the right hypochondriac region, vomiting, and weight loss since 45 days along with the history of loss of appetite and indigestion for 20 days. On examination, her vital parameters were within normal limits. Renal function test was within the normal limit. Hematological parameters revealed mildly raised. TLC was found, the 13,300 cells/mm3 . Biochemical investigation (liver function test) was shown deranged parameters in Table 1. Table 1: Liver function test Biochemical parameters Obtained value Normal reference Range S. Bilirubin Total Direct Indirect 13.1 mg/dl 2.0 mg/dl 11.1 mg/dl 0.3 – 1.0 mg/dl 0.0 to 0.2 mg/dl 0.4 to 0.8 mg/dl S.G.P.T. 108 U/L 5 – 42 U/L S.G.O.T. 130 U/L 5 – 40 U/L S. Alkaline phosphatase 1485 U/L 25 - 120 U/L USG findings of the patient revealed markedly distended gall bladder with thickened and edematous gallbladder wall and lumen was filled with multiple calculi. The proximal part of common bile duct not adequately visualized due to theedematous gallbladder wall. A Liver was mildly enlarged with intra-hepatic biliary channels slightly dilated. One month after cholecystectomy, CECT whole abdomen was performed which revealed multiple lymph nodes in peri-portal, peri-pancreatic, coeliac, pre-aortic, para-aortic, aorto-caval lymph nodes up to 1.5 cm- Lymph nodal secondaries. Also, there were mild as cites with mild hepatosplenomegaly. * CA 19.9 cancer marker was also done, which was found within normal limit. Gross- Cholecystectomy and hysterectomy specimen of the same patient were sent to the Pathology department of GSVM Medical College, Kanpur, in two separate jars for histopathological examination. JAR I was labeled gall bladder as Cholecystectomy specimen measured 8x4 and 5x2 cm. The outer surface showed few fibro fatty adhesions. On cut section, inner surface showed glistening mucosa with a greyish white area. Wall thickness varies from 1.5 to 2 cm. There were multiple stones inside the jar shown in Fig. 1 (A,B). Fig. 1 (A): Cholecystectomy specimen shows a greyish white area Fig. 1 (B): Cholecystectomy specimen shows a glistening mucosa on cut section JAR II was labeled total abdominal hysterectomy. The specimen consisted of the uterus, cervix with bilateral adnexa. Microscopy examination- Multiple H & E stained sections from gall bladder were examined shows marked thickening of gallbladder wall comprising of mucosa, muscular layer and serosa. B A
  • 3. SSR Inst. Int. J. Life Sci. Singh et al., 2019 DOI:10.21276/SSR-IIJLS.2019.5.1.12 Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2198 Numerous well-demarcated mucin pools with atypical cells (floating into the mucin pools) having a high nucleocytoplasmic ratio, moderate amount of vacuolated cytoplasm, were seen on the mucosal surface (Fig. 2 to Fig. 5). These mucin pools were surrounded by inflammatory cells infiltrate comprising of mature lymphocytes, macrophages and fibroblasts along with few congested and dilated blood vessels. These atypical cells and mucin pools were also in filtrating the muscle layer with similar picture and were also involving up to the serosa. Findings were suggestive of primary mucinous adenocarcinoma of gallbladder. Microscopic findings of received hysterectomy specimen were histopathologically normal. DISCUSSION Gallbladder carcinoma is the fifth most common G. I. malignancy [7] . It is a disease of elderly, more common in females than in males (3:1) and there are various types of gall bladder carcinoma such as adenocarcinoma, squamous cell carcinoma, adenosquamous carcinoma and very rare mucinous adenocarcinoma [5] . Mucinous carcinoma has two histologic variants. One with large pool of extracellular mucin with groups of tumour cells and other types with cystically dilated mucin filled glands. These may be present either alone or in combination [1] . In the majority of cases mucinous adenocarcinoma was frequently well-differentiated and admixed with conventional adenocarcinoma but poorly differentiated mucinous adenocarcinoma with distant metastasis can be found. Focal mucinous differentiation and well- differentiated adenocarcinoma with intra glandular mucin also occur [8] . Mucinous carcinoma constitutes only 2.5%. This was rather uncommon in gall bladder and is noted in the literature mostly as individual case reports or small handful of cases [6] . Presence of gall stones is one of the major risk factors for gallbladder adenocarcinoma, as in our case report but Fig. 2: Scanner view (4x) shows well-demarcated mucin pools Fig. 3: Low power view (10x) shows mucin pool surrounded by inflammatory cells infiltrate and few blood vessels Fig. 4: Low power view (10x) shows an involvement of serosa Fig. 5: High power view (40x) shows clusters of neoplastic cells floating in mucin
  • 4. SSR Inst. Int. J. Life Sci. Singh et al., 2019 DOI:10.21276/SSR-IIJLS.2019.5.1.12 Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2199 10-25% of patients with gall bladder carcinoma. They do not have associated cholelithiasis [9] . We can differentiate mucinous carcinoma from conventional gall bladder adenocarcinoma by MUC 2 positivity and from intestinal carcinoma by inverse CK7/CK20 profiles [10] CK7 (+) and CK20 (-) [11] . It was CDX2 (Negative) so can be differentiated from pancreatic mucinous carcinoma [12] . It was MUC6 (Negative) so can be differentiated from mammary colloid carcinoma [13] . Owing to the location of gallbladder, dissemination of tumor to adjacent tissue is usually present at the time of diagnosis. Most patients were not suitable for curative surgery because of advanced stage of the disease [7] . CONCLUSIONS Mucinous adenocarcinoma is a rare variant of gall bladder carcinoma. It has more aggressive behavior and worse prognosis than that of conventional adenocarcinoma of gall bladder. Most mucinous carcinoma is a mixed-mucinous, not pure colloid type. It is very essential to differentiate a primary mucinous adenocarcinoma from metastatic mucinous adenocarcinoma arising from other sites/organs because of different modes of treatment and different prognosis. Tumour markers have increasing significance in the diagnosis and evaluation of gall bladder carcinoma. Assay of carbohydrate antigen (CA) 242, carbohydrate antigen (CA) 15-3, carbohydrate antigen (CA) 19-9 and carbohydrate antigen (CA) 125 were fairly good markers for discriminating patients of carcinoma of the gall bladder from cholelithiasis. CA242 and CA125, when used together achieved best sensitivity and specificity. Serum markers seem to be less sensitive when used individually in carcinoma of the gall bladder but may prove useful in combination. ACKNOWLEDGMENTS The authors are highly grateful to the respective Universities and Principals of relevant Institutions to carry out the present investigations. CONTRIBUTION OF AUTHORS Research concept- Dr. Anveksha Sachan Research design- Dr. Neelima Verma Supervision- Dr. Anita Omhare Materials- Dr. Anita Omhare Data collection- Dr. Anita Omhare Data analysis and interpretation- Dr. Anita Omhare Literature search- Dr. Swetlana Sachan Writing article- Dr. Anveksha Sachan Critical review- Dr. Mahendra Singh Article editing- Dr. Anveksha Sachan Final approval- Dr. Anveksha Sachan REFERENCES [1] Albores SJ, Menck HR, Scoazec JC, Soehendra N, Wittekind C, Sriram PV, et al. Carcinoma of the gallbladder and extra hepatic bile ducts. In: Hamilton SR, Aaltonen LA, editors. WHO Classification of Tumors. Pathology and Genetics of Tumors of the Digestive system. Lyon: IARC Press, 2000; pp. 206-12. [2] Adsay VN, Klimstra DS. Benign and malignant Tumors of gall bladder and extra hepatic biliary tract. In: Odze RD, Goldblum JR, editors. Surgical pathology of the GI tract, liver, biliary tract and pancreas. 2nd ed. Philadelphia: Saunders Elsevier 2009; pp. 857-70. [3] Adsay VN. Gall Bladder, Extra hepatic biliary Tree, and Ampulla. In: Mills SE, editor. Sternberg’s Diagnostic surgical pathology. 5th ed. Lippincott Williams and Wilkins, 2010; pp. 1620-24. [4] [1] Gupte PA, Chaturvedi R, Patil LY, Joshi AS. Pure mucinous (Colloid) adenocarcinoma of the Gall bladder– A rare phenotype. Oncol. Gastroenterol. Hepatol. Reports, 2013; 2(1): 27-29. [5] Misra S, Chaturvedi A, Misra NC, Sharma ID. Carcinoma of gall bladder. Lancet oncol., 2003; 4(3): 167-76. [6] Tangde AR, Rathod SG, Joshi AR, Bindu RS. Mucinous adenocarcinoma of gall bladder: A case report. Int. J. Res. Med. Sci., 2017; 5(11): 5082–84. [7] Abd-Allah MA, Ali MHM, Khalid OI, Gazali M, Dr M. Allata AA. Mucinous Adenocarcinoma of the Gallbladder: A Case Report. Int. J. Multidisciplinary Curr. Res., 2016; 4: 37-38. [8] Singh M, Vishwakarma I, Purwar N, Verma YN, Sharma T. Mucinous carcinoma of Gall Bladder an incidental Finding of a rare case. Int. J. Life Sci. Scient. Res., 2017; 3(5): 1411-14. [9] Dursun N, Escalona OT, Roa JC, Basturk O, Bagci P, et al. Mucinous carcinoma of Gall bladder: Clinicopathologic analysis of 15 cases identified in 606 carcinomas. Arch. Pathol. Lab. Med., 2012; 136(1): 1347-58.
  • 5. SSR Inst. Int. J. Life Sci. Singh et al., 2019 DOI:10.21276/SSR-IIJLS.2019.5.1.12 Copyright © 2015 - 2019| SSR-IIJLS by Society for Scientific Research under a CC BY-NC 4.0 International License Volume 05 | Issue 01 | Page 2200 [10]Allah AAM, Ali MHM, et al. Mucinous Adeno carcinoma of gall bladder: A case report. Int. J. multidisciplinary Curr. Res., 2016; 4: 37–38. [11]Mills SE, Greenson JK, et al. Surgical histopathology Sternberg’s 6th edition; 2015; 1797-1802. [12]Miller SE, Greenson JK, et al. Surgical histopathology Sternberg’s 6th Ed: 2015, pp. 1617. [13]Rosai J. Ackerman’s surgical pathology Rosai & Ackerman’s. 10th Ed: 2012, pp. 1700. Open Access Policy: Authors/Contributors are responsible for originality, contents, correct references, and ethical issues. SSR-IIJLS publishes all articles under Creative Commons Attribution- Non-Commercial 4.0 International License (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/legalcode