OPEN ACCESS  
CASE REPORT  
Large Diffuse Cutaneous Metastases Secondary to Rectal  
Mucinous Adenocarcinoma  
Agustín A. Alesandrini1, Isidro Moggiano2, Juan A. Perriello1, Tomás F. Ferrer Quiroga2  
1Colorectal Surgeon  
2General Surgery Resident  
Hospital Privado de La Comunidad, Mar del Plata, Argentina  
ABSTRACT  
Cutaneous metastases as the initial manifestation of colorectal cancer are rare, with an incidence below 1%. They usually occur  
in patients with advanced disease and may present with variable clinical features mimicking infectious conditions. Early recognition  
is essential for timely diagnosis and appropriate management.  
We report the case of an immunosuppressed kidney transplant recipient who developed cutaneous lesions initially suspected to  
be herpes zoster. Owing to the lack of response to antiviral therapy, a skin biopsy was performed and revealed metastatic  
mucinous carcinoma. Immunohistochemical findings supported a colorectal origin, and imaging studies identified a primary rectal  
tumor with metastatic disease.  
To cite:  
Alesandrini AA, Moggiano I, Perriello JA,  
Ferrer Quiroga Tomás F. Large Diffuse  
Cutaneous Metastases Secondary to Rectal  
Mucinous Adenocarcinoma. Rev Argent  
Coloproctol. 2026; 37(2):25-28.  
doi:10.46768/bzhrdb11  
This case highlights the importance of including cutaneous metastases in the differential diagnosis of atypical skin lesions,  
particularly in immunocompromised patients, and underscores the pivotal role of biopsy and immunohistochemistry in identifying  
neoplasms of initially unknown origin.  
u
Additional supplemental material, when  
applicable, is published online only. To view,  
please visit the journal online:  
Keywords: cutaneous metastases; colorectal cancer; mucinous adenocarcinoma; immunosuppression; herpes zoster  
Received: November 10, 2025  
Accepted: April 28, 2026  
evaluation. She was receiving immunosuppressive  
INTRODUCTION  
therapy with sirolimus (2 mg/day) and  
methylprednisolone (4 mg/day). Her medical history  
Cutaneous metastases from colorectal cancer are an  
was also notable for neuropathy, peripheral arterial  
uncommon manifestation, with a reported incidence  
disease, and right above-knee amputation.  
of less than 1% among affected patients.1–3 Within  
The patient presented with painful vesicular lesions  
the spectrum of cutaneous metastases arising from  
involving the right lower extremity stump, initially  
solid tumors, colorectal cancer represents  
a
interpreted as herpes zoster in the setting of  
immunosuppression (Fig. 1). However, because of  
the lack of response to antiviral therapy and  
relatively rare etiology compared with malignancies  
more commonly associated with skin involvement,  
such as breast and lung cancer.³  
persistence of the lesions,  
performed.  
a
skin biopsy was  
Clinically, these lesions demonstrate marked  
morphologic heterogeneity. They may present as  
firm subcutaneous nodules, infiltrative plaques, or,  
less frequently, as atypical lesions mimicking  
infectious processes such as herpes zoster.⁴ This  
broad clinical spectrum may complicate diagnosis  
and delay appropriate treatment, particularly in  
immunocompromised patients.  
Histopathologic examination revealed dermal  
infiltration by neoplastic cells suspended within  
abundant extracellular mucin, forming characteristic  
mucin pools consistent with mucinous carcinoma  
(Fig.  
2).  
Immunohistochemical  
analysis  
demonstrated positivity for cytokeratins AE1/AE3,  
CK20, and CDX2, and negativity for CK7, TTF1,  
PAX8, CD10, and GATA3, findings consistent with  
cutaneous metastasis of colorectal origin.  
Given the suspicion of metastatic disease from an  
initially unknown primary tumor, CT of the chest,  
abdomen, and pelvis was performed, demonstrating  
irregular mural thickening of the lower rectum,  
The presence of cutaneous metastases generally  
reflects advanced systemic dissemination and is  
associated with a poor prognosis, with a reported  
median survival of less than 1 year from the time of  
2026 The authors. Published by Revista  
Argentina de Coloproctología. This article is  
distributed under the Creative Commons  
Attribution–NonCommercial–NoDerivatives  
4.0 International License (CC BY-NC-ND  
4.0)  
,
diagnosis.⁴ ⁵ In this setting, early recognition is  
essential, as it may facilitate timely therapeutic  
optimization and guide appropriate clinical  
management.  
Mucinous rectal carcinoma represents a distinct  
histologic subtype characterized by abundant  
extracellular mucin production and unique biologic  
mesorectal,  
retroperitoneal,  
and  
inguinal  
nc-nd/4.0/  
lymphadenopathy measuring up to 26 mm (Fig. 3),  
as well as multiple pulmonary nodules suggestive of  
metastatic disease.  
Endoscopic evaluation and rectal MRI were not  
performed due to the patient’s clinical condition and  
the confirmed tumor origin based on histopathologic  
and imaging findings.  
Microsatellite instability testing was not performed  
because the patient was not considered a candidate  
for immunotherapy given her immunosuppressed  
status.  
behavior, including  
a
greater propensity for  
peritoneal dissemination and differential therapeutic  
response patterns compared with conventional  
adenocarcinoma.⁶ Although cutaneous involvement  
is exceedingly rare, its recognition may represent the  
first manifestation of metastatic disease or tumor  
progression.  
Correspondence to  
Agustín A. AlesandrinI  
The case was discussed at a multidisciplinary tumor  
board, and systemic treatment with capecitabine was  
initiated. After 3 cycles of chemotherapy, disease  
stabilization was observed in both the cutaneous  
lesions and the primary tumor. However, tumor  
progression was confirmed 8 months after diagnosis,  
leading to a transition to palliative and symptom-  
directed care. The patient died 11 months after the  
initial diagnosis.  
CASE  
An 81-year-old woman with a medical history  
significant for hypertension, chronic kidney disease  
secondary to polycystic kidney disease, and  
deceased-donor kidney transplantation performed in  
2011 with preserved graft function presented for  
REV ARGENT COLOPROCT | 2026 | VOL 37, No. 2  
CASE REPORT  
infections are more prevalent. In the present case, the initial  
suspicion of herpes zoster in a renal transplant recipient illustrates  
this diagnostic challenge.  
Immunosuppression is a relevant factor in this context, not only  
due to the increased risk of de novo malignancies in transplant  
recipients, but also because of the potential for atypical and more  
aggressive clinical presentations.10 This underscores the  
importance of maintaining a high index of suspicion for persistent  
or atypically evolving cutaneous lesions in this population.  
Histopathology and immunohistochemistry play a central role in  
determining tumor origin, particularly when the primary tumor  
has not been previously identified. The presence of mucin lakes  
containing floating neoplastic cells, together with an  
immunoprofile characterized by CK20 and CDX2 positivity and  
CK7 negativity, supports a colorectal origin and helps exclude  
other common primary sites such as lung, breast, kidney, or  
gynecologic tumors.  
Figure 1. Vesicular cutaneous lesions on the right lower extremity stump,  
initially interpreted as herpes zoster.  
DISCUSSION  
Cutaneous metastases from colorectal carcinoma are an  
uncommon manifestation, with a reported incidence of less than  
1% of cases, and typically reflect advanced systemic disease.1–3  
In most patients, they occur in the setting of known metastatic  
disease; therefore, their presentation as an initial manifestation or  
as a finding leading to the diagnosis of the primary tumor is  
exceptional.  
From a clinical standpoint, colorectal cutaneous metastases most  
frequently involve the abdominal wall, perineal region, and  
surgical scars, a distribution associated with mechanisms of direct  
extension or tumor implantation.4,7 However, less common sites  
have also been reported, including the chest, head and neck, and  
extremities; the latter represent a particularly rare presentation, as  
-
observed in the present patient.⁷ ⁹  
Figure 3. CT scan of the abdomen and pelvis showing irregular mural  
thickening of the lower rectum with associated inguinal lymphadenopathy.  
Regarding prognosis, the development of cutaneous metastases in  
colorectal cancer is associated with limited survival, with  
reported medians ranging from 5 to 12 months from diagnosis.4,5  
Although treatment of colorectal cutaneous metastases is  
predominantly palliative,  
a
multidisciplinary approach may  
contribute to improved symptom control and quality of life. In the  
present case, systemic chemotherapy with capecitabine initially  
achieved disease stabilization; however, tumor progression was  
subsequently observed at 8 months after diagnosis, with an  
overall survival of 11 months, consistent with the published  
literature.  
This case adds several clinically relevant aspects to the existing  
literature, including metastatic involvement of an extremity, a  
pseudozosteriform clinical presentation, and the context of  
immunosuppression in  
highlights the importance  
a
renal transplant recipient. It also  
of integrating clinical,  
histopathological, and imaging findings to achieve an accurate  
diagnosis and guide appropriate therapeutic management.  
CONCLUSIONS  
The presence of atypical, persistent, or unusually evolving  
cutaneous lesions, particularly in immunocompromised patients,  
should raise suspicion for metastatic involvement, even when the  
clinical presentation mimics common infectious entities such as  
herpes zoster.  
Skin biopsy, complemented by histopathologic and  
immunohistochemical analysis, represents the key diagnostic tool  
for determining tumor origin in neoplasms with an initially  
unknown primary site.  
Figure 2. Histopathology of the cutaneous lesion. A. Preserved epidermis  
with dermal infiltration by neoplastic cells associated with abundant  
extracellular mucin, consistent with mucinous adenocarcinoma (H&E,  
40×). B. Tumor cells arranged in clusters within extracellular mucin  
pools, showing vesicular nuclei and prominent nucleoli (H&E, 400×).  
This case underscores the importance of a comprehensive  
multidisciplinary diagnostic approach and the consideration of  
uncommon differential diagnoses in atypical clinical  
presentations. The integration of clinical, histopathological, and  
imaging findings is essential to guide therapeutic decision-  
While nodular lesions are the most common clinical presentation,  
atypical variants that may mimic infectious or inflammatory  
conditions, including zosteriform patterns, have also been  
described.4,8 This phenomenon may lead to diagnostic delays,  
particularly in immunocompromised patients, in whom cutaneous  
DIFFUSE CUTANEOUS METASTASES SECONDARY TO RECTAL MUCINOUS ADENOCARCINOMA  
Alesandrini AA, et al.  
REV ARGENT COLOPROCT | 2026 | VOL 37, No. 2  
CASE REPORT  
2. Krathen RA, Orengo IF, Rosen T. Cutaneous metastasis: a meta-analysis  
of data. South Med J. 2003;96(2):164–7.  
3. Brenner M, Zalaudek I, Hofmann-Wellenhof R. Cutaneous metastases of  
internal malignancies: an update. J Dtsch Dermatol Ges. 2020;18(8):816–  
27.  
making and optimize the management of patients with advanced  
malignancy.  
Author Contributions  
4. Nashan D, Müller ML, Braun-Falco M, Reichenberger S, Szeimies RM,  
Bruckner-Tuderman L. Cutaneous metastases of visceral tumours:  
review. J Cancer Res Clin Oncol. 2009;135(1):1–14.  
5. Wang DY, Ye F, Lin JJ, Xu X. Cutaneous metastasis: a rare phenomenon  
of colorectal cancer. Ann Surg Treat Res. 2017;93(5):277–80.  
6. Hugen N, van de Velde CJH, de Wilt JHW, Nagtegaal ID. Mucinous  
colorectal carcinoma: clinical pathology and treatment options. Ann Surg  
Oncol. 2015;22(11):3499–505.  
7. Parente P, Ciardiello D, Reggiani Bonetti L, Famiglietti V, Cazzato G,  
Caramaschi S, et al. Cutaneous metastasis from colorectal cancer: making  
light on an unusual and misdiagnosed event. Life (Basel).  
2021;11(9):954.doi: 10.3390/life11090954.  
8. Chiang A, Hsu CK, Lee JY. Cutaneous metastasis mimicking herpes  
zoster: a case report and review of the literature. Dermatol Online J.  
2018;24(2):13030.  
AAA: conceptualization, methodology, research, drafting of the original  
manuscript, revision, and editing of the manuscript. IM: conceptualization,  
methodology, research, drafting of the original manuscript. JAP: supervision,  
project management, and manuscript revision. TFFQ: research, resources,  
and collection and curation of material. All authors approved the final version  
of the manuscript.  
a
Conflict of interest statement: None  
Funding: None  
Data availability statement: The data are publicly available  
ORCIDS  
Agustin A. Alesandrini: 0000-0002-9821-8360  
Juan A. Perriello: 0000-0002-2739-7242  
Tomás F. Ferrer Quiroga: 0009-0004-9361-6492  
9. Zelenova E, Belysheva T, Sofronov D, Semenova V, Radjabova G,  
Vishnevskaya Y, et al. Cutaneous metastasis of rectal cancer as a diagnostic  
challenge:  
a
clinical case and literature review. Diagnostics (Basel).  
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DIFFUSE CUTANEOUS METASTASES SECONDARY TO RECTAL MUCINOUS ADENOCARCINOMA  
Alesandrini AA, et al.