Abstract
Clown nose-like lesion refers to the manifestation of a reddish or skin-colored bulge on the tip of the nose or the manifestation of bulbous tip of the nose. More and more clinical cases show that clown nose-like lesion can also be the indication of some genetic syndromes, not just the manifestation of metastatic visceral tumor as it initially proposed. However, the clinical features of clown nose-like lesion indicated by metastatic malignancies, genetic cancer predisposition syndromes or primary diseases involving the nasal tip are lacking. In this study, patients with clown nose-like lesion in our clinical practices and from published literatures were collected and reviewed. We found that clown nose-like lesions caused by metastatic malignancies including lung cancer are often solitary and more common in male (24/31) older individuals (average age 62.3, ranging 40–78 years old). In addition, they usually appear for a short time, and are prone to be misdiagnosed as primary nasal diseases, leading to a poor prognosis (all patients with data available died within 4 months). Clown nose-like lesions associated with genetic cancer predisposition syndromes usually develop at a young age (mean age 15.3) with female preference (9/10). They are accompanied by multiple-systemic involvements, including low hair volume, developmental delay, cancer predisposition or neurological diseases. They show slow development and often positive family history (6/10). These two kinds of clown nose-like lesions are often asymptomatic, which delays the diagnosis and treatment of underlying malignancies or syndromes. In brief, the term of clown nose-like lesion is underrecognized, and should be updated. Clown nose-like lesions can serve as indicators to at least three categories of clinical issues: metastatic visceral tumors, genetic syndromes, and primary diseases involving the nasal tip. Increased awareness of clinical features of updated clown nose-like lesions can alert physicians to these underlying malignancies or syndromes, render earlier detection of associated medical issues, and allow for genetic counseling of family members.
Keywords: skin metastases, lung cancer, genetic syndromes, manifestation, nose, clown nose-like lesion
Introduction
Clown nose-like lesion refers to the manifestation of a reddish or skin-colored bulge on the tip of the nose or the manifestation of bulbous tip of the nose, resembling the fake nose of a clown (1). Initially, clown nose-like lesion was considered as a indicator of cutaneous metastatic malignancies, including lung cancer (2), renal clear cell carcinoma (3), rhabdomyosarcoma (4), cervical cancer (5), and liver cancer (6). In clinical practice, however, it can also be a cue for genetic syndromes, such as Tricho-Rhino-Phalangeal syndrome (7), as well as some primary nasal diseases including infections such as leishmaniasis (8), inflammations such as rosacea (9), and tumors such as keratoacanthoma (10).
In this study, patients with clown nose-like lesions in our clinical practices and from published literatures were collected and reviewed. They were divided into three categories: metastatic visceral tumors, genetic syndromes, and primary diseases involving the nasal tip. Detailed clinical features on the gender, age, skin lesion characteristics, nasal skin lesion symptoms, initial diagnosis, and outcome of these cases were analyzed. Increased awareness of these clinical features of updated clown nose-like lesions can alert physicians to the underlying malignancies or genetic syndromes, and render earlier detection of associated medical comorbidities.
Methods
Patients
We collected clinical cases with clown nose-like lesions who were admitted to our dermatology departments. Their initial diagnoses were made by a dermatologist at admission, and confirmed/corrected by three independent dermatologists with the help of histopathology and/or medical imaging. This clinical case survey was approved by Medical Ethics Committee in Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital.
Literature Review
Published cases with clown nose-like lesions were retrieved from the databases of PubMed and Google Scholar. Medical Subject Heading (MeSH) included “nose” or “nasal” combined with “syndrome,” “genetic,” “cancer,” “tumor,” or “carcinoma.” Only articles published in English were included.
Data Analysis
These cases were divided into three categories: metastatic visceral tumors, genetic syndromes, and primary diseases involving the nasal tip. Their medical records were collected and reviewed. Detailed clinical features on the gender, age, skin lesion characteristics, nasal skin lesion symptoms, initial diagnosis, and outcome of these cases was analyzed.
Results
Demographic and Clinical Characteristics
In total, 31 cases with clown nose-like lesions from metastatic visceral tumors and 10 cases with clown nose-like lesions from genetic syndromes, as well as 20 kinds of primary diseases involving the nasal tip, were collected (Figure 1). Their detailed demographic information and clinical characteristics were displayed in Tables 1–4.
Figure 1.
Clinical images of clown nose-like lesions. (A–D) Clown nose-like lesions secondary to metastatic visceral tumors. (A) A 65-year-old man with lung squamous cell carcinoma (case 4 in Table 1), initially misdiagnosed as rosacea; (B,C) a 65-year-old man with lung squamous cell carcinoma (case 2 in Table 1), initially misdiagnosed as folliculitis; (D) a 63-year-old woman with lung squamous cell carcinoma (case 1 in Table 1), initially misdiagnosed as basal cell carcinoma. (E–H) Clown nose-like lesions nose as manifestations of genetic syndromes. (E) A 34-year-old woman with tuberous sclerosis (case 6 in Table 3); (F) a 40-year-old woman with multiple familial trichoepithelioma (case 5 in Table 3); (G) a 85-year-old woman with Brooke-Spiegler syndrome (11); (H) a 13-year-old girl with Tricho-Rhino-Phalangeal Syndrome in our department. (I–L) Primary skin disease of clown nose-like lesions. (I) A 47-year-old man with sebaceous gland hyperplasia (case 12 in Table 4); (J) a 62-year-old woman with superficial skin mycosis (case 8 in Table 4); (K) a 42-year-old man with rosacea (case 10 in Table 4); (L) a 34-year-old man with nasal squamous cell carcinoma (case 9 in Table 4).
Table 1.
Nasal tip cutaneous metastasis from lung carcinoma.
| Sex/Age | Description of nasal lesion | Course of clown nose-like lesion | Initial diagnosis | Lung histopathology | Prognosis | References |
|---|---|---|---|---|---|---|
| F/76 | A blue-black spherical mass | N/A | Haemangioma | Oat cell carcinoma | Died in 3 M | (12) |
| M/67 | A subcutaneous lump | 4 M | Rhinophyma | Squamous cell carcinoma | N/A | (12) |
| M/71 | N/A | N/A | Rosacea | Squamous cell carcinoma | Died immediately | (13) |
| M/65 | Enlarging nasal tip | 4 W | Cellulitis | Adenosquamous cell carcinoma | Died in several weeks | (14) |
| M/58 | Nodules | 1 M | Metastatic tumor | Not described | Died in 3 M | (15) |
| M/63 | N/A | N/A | Tumor | Anaplastic large cell carcinoma | Died in 2 W | (16) |
| M/59 | Nodules | 6 W | Mass | Squamous cell carcinoma | N/A | (17) |
| M/64 | A cutaneous tumor | 3 M | Furuncle | Large cell undifferentiated carcinoma | Died in 6 M | (18) |
| M/74 | Fuchsia nodules | N/A | Folliculitis | Squamous cell carcinoma | Died in 3 M | (19) |
| M/62 | A round erythematous nodule | 5 W | Tumor | Squamous cell carcinoma | Died in 5 M | (2) |
| M/76 | A round erythematous tumor | 4 M | Rhinophyma | Squamous cell carcinoma | Died in 1 M | (2) |
| M/57 | Tender, oval and erythematous nodules | 1 M | Rhinophyma | Squamous cell carcinoma | Died in 9 M | (2) |
| F/63 | Pale pink patches and black scabs | 1 M | Basal cell carcinoma | Squamous cell carcinoma | Died in 6 M | Our case 1 |
| M/65 | Red nodules with clear border | 5 W | Folliculitis | Squamous cell carcinoma | Died in 7 M | Our case 2 |
| M/70 | Cauliflower-like mass | 2 M | Metastatic tumor | Squamous cell carcinoma | Died in 2 M | Our case 3 |
| M/65 | Red nodule | <1 M | Rosacea | Squamous cell carcinoma | N/A | Our case 4 |
“F” and “M,” female and male in Sex column; “Y,” “M,” and “W,” year, month, and week in course of clownlike nose column; “N/A,” data not available.
Table 4.
Primary diseases that can present with clown nose-like lesions.
| Classification | Diseases | Nasal symptoms | Diagnosis | References |
|---|---|---|---|---|
| Infection | Cutaneous Leishmaniasis | Erythema, verrucous hyperplasia | Identification of Leishmania by smear or culture | (37) |
| Blastomycosis | Verrucous nodules | Histopathology | (38) | |
| Deep skin mycosis | Erythema, papules, scabs | Microscopic examination or culture of fungi | Our case 7 | |
| Superficial skin mycosis | Erythema, papules, scaling | Microscopic examination or culture of fungi | Our case 8 | |
| Tumor-associated | Basal cell carcinoma | Erythema, plaque, ulcer | Histopathology | (39) |
| Squamous cell carcinoma | Plaque, verrucous hyperplasia, central ulcer | Histopathology | Our case 9 | |
| Keratoacanthoma | Papules, nodules | Histopathology | (10) | |
| Sebaceous carcinoma | Light red nodules | Histopathology | (40) | |
| Trichoblastoma | Nodules | Histopathology | (41) | |
| Microcystic adnexal carcinoma | Yellow or red nodules | Histopathology | (42) | |
| Cutaneous T-cell lymphoma | Scabs, bloody discharge | Histopathology | (43) | |
| Rhabdomyosarcoma | Smooth surface, red hard patches | Histopathology | (44) | |
| Folliculosebaceous cystic hamartoma | Tawny skin mass | Histopathology | (45) | |
| Cutaneous sinus histiocytosis | Papules, nodules | Histopathology | (46) | |
| Inflammation | Rosacea | Erythema, nodules, and nasal glands | Clinic | Our case 10 |
| Acne | Nodules, cysts | Clinic | Our case 11 | |
| Others | Sebaceous gland hyperplasia | Light-red or light-yellow nodular hyperplasia | Histopathology | Our case 12 |
| Pseudolymphoma | Red smooth hard nodules | Histopathology | (26) | |
| Sinonasal sarcoidosis | Papules, nodules | Histopathology | (47) | |
| Juvenile xanthogranuloma | Yellow-red nodules | Histopathology | (48) |
“N/A,” data not available.
Clown Nose-Like Lesions Secondary to Metastatic Visceral Tumors
Nasal Tip Cutaneous Metastasis From Lung Carcinoma
Internal malignant tumors can metastasize to other organs including the skin (49, 50). When looking up the frequency of metastasis of lung carcinomas, there are some preferential sites, as the bone 34.3%, the brain 28.4%, the adrenals 16.7%, and the liver 13.4%, depending on the availability of research data (51). Lung carcinoma metastasis to the skin, especially the nose, is rare and easily overlooked.
In this study, a total of 16 cases of lung cancer metastasis with clown nose-like lesions were collected (Table 1). We found they usually presented as active or fixed, hard or soft, single or multiple, painless nodules. They had a variety of colors, ranging from flesh-colored to red-purple, blue-black, and they ranged in diameter from 5 mm to 6 cm (Figure 1). The average age of the 16 cases was 65.9 (ranging 57–76 years old), indicating that lung cancer and its nasal metastasis have a higher incidence in older individuals. Only two of the 16 cases were women. Considering that the incidence of lung cancer is not much different between men and women (52), it further indicated that nasal metastasis may be more likely to occur in male (14/16) older lung cancer patients (average age 65.4). In addition, most lung cancer patients (11/16) with clown nose-like lesions have been demonstrated to be metastatic squamous cell carcinoma by histopathology. Moreover, the nose is the most noticeable area of the face, and patient with nasal involvement are more likely to present to a dermatology clinic, while ignoring the signs and symptoms that accompany systemic diseases, especially when there is no history of internal malignancies. In this study, we showed that clown nose-like lesions usually appear for a short time (<2 months), and most cases (14/16) were misdiagnosed as primary nasal skin diseases, especially rosacea or furuncle, at the first visit. Finally, the prognosis of lung cancer with skin metastasis is poor. Skin metastases are usually accompanied by internal metastases in other organs, such as brain, liver, bone and adrenal glands (our Case 3). It has been reported that the average survival time after metastasis was 5 months (53). In this retrospective analysis, patients died about 4 months after the diagnosis of clown nose-like lesion metastasis, suggesting poorer prognosis (Table 1).
Nasal Tip Cutaneous Metastasis From Other Carcinomas
In addition to the 16 cases of lung cancer metastasis mentioned above, we analyzed 15 cases suffering from nasal metastasis secondary to renal clear cell carcinoma, rhabdomyosarcoma, cervical cancer, chordoma, liver cancer, acute myeloid leukemia, basal laryngeal squamous cell carcinoma, squamous cell carcinoma of the larynx, thyroid cancer, hypopharyngeal cancer, hypopharyngeal squamous cell carcinoma, esophageal squamous cell carcinoma and esophageal cancer, respectively (Table 2). In these cases, the course of clown nose-like lesion lasted from several weeks to 1 year (mean 3 months), and nasal manifestations usually appeared as swelling, purplish red bumps or nodules. Similar to lung cancer metastasis, patients with clown nose-like lesions secondary to these cancers were usually older than 50 (average age 55.1, ranging 6–78 years old), especially male (10/15) older patients (average age 58, ranging 40–78 years old). When we put all the tumors together (Tables 1, 2), we can still find gender preference of clown nose-like lesion in male elderly (24/31, average age 62.3, ranging 40–78 years old).
Table 2.
Nasal tip cutaneous metastasis from other carcinomas.
| Sex/Age | Primary tumor | Nasal lesions | Course of clownlike nose | Chief complaint organ at first visit | Treatment | Prognosis | References | |
|---|---|---|---|---|---|---|---|---|
| Nasal tip | System therapy | |||||||
| F/55 | Renal clear cell carcinoma | Vascular erythema, papules | 1 Y | Kidney | N/A | Local radiotherapy | N/A | (3) |
| F/6 | Rhabdomyosarcoma of nasal cavity | Nose lumps | 6 M | Nasal tip | resection | Partial resection | N/A | (4) |
| F/48 | Cervical cancer | Purple-red and swollen; dilated capillaries | 3 M | Nasal tip | Local radiotherapy | Resection | Purplish redness faded after 5 years | (5) |
| F/64 | Cervical cancer | Swelling | 3 M | Cervix | Radiotherapy | Surgery plus radiotherapy | Died after 3 M | (20) |
| M/40 | Sacrococcygeal chordoma | Small hard nodules | 2 M | Spine | N/A | N/A | N/A | (21) |
| M/78 | Liver cancer | Violet bump | N/A | N/A | N/A | N/A | Died after 20 M | (6) |
| M/18 | Acute myeloid leukemia | Violet nodules, bumps | 1 M | N/A | N/A | Chemotherapy | Getting well gradually | (22) |
| M/72 | Basal laryngeal squamous cell carcinoma | Tumors prone to bleeding | N/A | Throat | N/A | Surgery, radiotherapy and chemotherapy | Died after 2 M | (23) |
| M/77 | Squamous cell carcinoma of the larynx | Nose lumps | 3 M | Throat | Partial resection | Radiotherapy or chemotherapy | N/A | (24) |
| M/54 | Thyroid cancer | N/A | 2 M | Neck | N/A | Chemotherapy | Died after 2 M | (25) |
| M/74 | Hypopharyngeal cancer | Red nodules | 2 W | Hypopharynx, esophagus | N/A | Chemotherapy, surgery and radiotherapy | N/A | (26) |
| M/54 | Hypopharyngeal squamous cell carcinoma | Dilation of nasal capillaries, central ulcer | 2 M | Hypopharynx | N/A | Chemotherapy | N/A | (27) |
| F/74 | Esophageal squamous cell carcinoma | Painless violet-like red nodules | 6 W | Esophagus | N/A | N/A | N/A | (28) |
| M/54 | Esophageal squamous cell carcinoma | Dilated nasal blood vessels and central necrosis | N/A | Esophagus | Surgery | Surgery, radiotherapy | N/A | (29) |
| M/59 | Esophageal cancer | Hemispherical mass with clear boundaries | N/A | Nasal tip | N/A | Chemotherapy | Died after 18 M | (30) |
“F” and “M,” female and male in Sex column; “Y,” “M,” and “W,” year, month, and week in course of clownlike nose column; “N/A,” data not available.
The primary tumors were diagnosed first in most cases (12/15 cases), however, in some cases like the nasal tip metastasis from rhabdomyosarcoma, cervical cancer, and esophageal cancer in Table 2, the diagnosis of clown nose-like lesion even preceded the primary tumors. Consistent with those in lung cancers, clown nose-like lesions in these tumors also indicate poor prognosis, and patients died about 9 months after the diagnosis of clown nose-like lesion metastasis.
Clown Nose-Like Lesion as a Manifestation of Genetic Syndromes
Nasal lesions can also be as a manifestation of some genetic syndromes. We collected or referred to 10 cases of genetic syndromes with clown nose-like lesions, including Hernandez syndrome, Tricho-Rhino-Phalangeal Syndrome type I, multiple familial trichoepithelioma, tuberous sclerosis, and Brooke-Spiegler Syndrome (Table 3 and Figure 1). All cases developed nasal manifestations at a young age (mean 15.3 years old). Nine of them were women, suggesting a possible female predilection. Their nasal lesions usually presented as multiple hypertrophic nodules or papules, except for bulbous tip of the nose in patients of Tricho-Rhino-Phalangeal Syndrome type I. In addition, clown nose-like lesions were always accompanied by other obvious characteristics, such as cancer predisposition, sparse hair, intellectual problems, and/or neurological diseases (e.g., epilepsy).
Table 3.
Clown nose-like lesion as a manifestation of genetic syndromes.
| Sex/Age | Diagnosis | Characteristics of nasal lesions | Time of skin lesion | Involvement other than nose | Family history | References |
|---|---|---|---|---|---|---|
| F/16 | Hernandez syndrome | A large bulbous nose with thickened alae nasi and septum | Since age 8 | Convulsive disorder, psychomotor retardation, and obesity | N/A | (31) |
| F/4 | Multiple familial trichoepithelioma | Multiple round smooth translucent solid nodules and papules | Since age 2 | N/A | Grandmother and mother | (32) |
| F/40 | Multiple familial trichoepithelioma | Numerous flesh-colored round solid nodules and papules | Since age 10 | Trichoblastic carcinoma | Mother | Our case 5 |
| F/8 | Tricho-Rhino-Phalangeal Syndrome-I | Round nose | Since age 8 | Short and sparse hair, sparse outer eyebrows, short stature, thin nails, and curved fingers | Mother and grandmother | (33) |
| M/4 | Tricho-Rhino-Phalangeal Syndrome-I | Thick and pear-shaped nose | Since age 4 | Thinning hair, thinning of the outer eyebrows, thin upper lip, premature fusion of the epiphyses, difficulty in eating since childhood | N/A | (7) |
| F/1.4 | Tricho-Rhino-Phalangeal Syndrome-I | Spherical nasal tip | After birth | Growth retardation after birth, sparse hair, thin upper lip, prominent ears and forehead, small chin, short hands, and feet | Grandfather, uncle and mother | (34) |
| F/34 | Tuberous sclerosis | Light red rice grains to pea-sized hard pimples | Since age 30 | Mental retardation, epilepsy, hemoptysis, multiple subungual fibromas, multiple hamartomas of the liver and kidney, pulmonary lymphangiomyomatosis | Mother and son | Our case 6 |
| F/15 | Tuberous sclerosis | Pale red verrucous papules | Since age 10 | Mental retardation, epilepsy, multiple fibromas. Brain MRI and CT showed several cortical and subcortical nodules, subependymal nodules | N/A | (35) |
| F/26 | Tuberous sclerosis | Pale red pimples | Since age 26 | Epilepsy, brain imaging showed multiple cortical nodules and cortical malformations, but no subependymal nodules. Torso CT showed bilateral lumbosacral joint sclerosis | Two sisters have epilepsy | (36) |
| F/85 | Brooke-Spiegler syndrome | Multiple papulonodular lesions, increasing in number over the years | Since age 55 | Metastatic cylindrocarcinoma | N/A | (11) |
“F” and “M,” female and male in Sex column; “Y,” “M,” and “W,” year, month, and week in course of clownlike nose column; “N/A,” data not available.
Primary Diseases That Can Present With Clown Nose-Like Lesions
Primary diseases with clown nose-like lesions may be related to infections, inflammations, tumors, and other associated diseases (Table 4 and Figure 1). These diseases may present with nasal manifestations such as erythema, papules or nodules, and can be diagnosed through clinical features or laboratory tests. Clown nose-like lesions caused by infections or inflammations are relatively easy to diagnose via pathogen or clinic identifications. Neoplasm-associated clown nose-like lesions were common among middle-aged and elderly patients. However, for neoplasm-associated clown nose-like lesions, it was difficult to judge whether the tumor was benign or malignant, nor primary or secondary only by nasal manifestations. In this case, tissue biopsy and a thorough history including a review of systems were necessary to help make the final clinical diagnosis.
Discussion
The clown nose-like lesion is a term that refers to the manifestation of a reddish or skin-colored bulge on the tip of the nose or the manifestation of bulbous tip of the nose (1). Although clown nose-like lesion had been classically considered an indicator of cutaneous metastatic malignancies (e.g., lung cancer), there can be various other causes. Therefore, clinical issues behind clown nose-like lesions need to be considered comprehensively. In this study, patients with clown nose-like lesions in our clinical practices and from published literatures were collected. They were divided into three categories and reviewed: metastatic visceral tumors, genetic syndromes, and primary diseases involving the nasal tip.
For primary diseases with clown nose-like lesions, we classify them by infectious diseases, neoplasm-related diseases, inflammatory diseases, and other diseases. Infectious diseases have no obvious age tendency. The patient's living area or occupation should be noted whether it is possible to come into contact with animals or parasites. It's often necessary to rely on pathogenic examination or histopathological examination to help the diagnosis. Primary neoplastic diseases are usually found in patients with more than 50 years old. Ulcers may also present alongside the nasal nodules. The type of tumor needs to be confirmed by histopathological examination. Inflammatory diseases, such as rosacea, are common diseases. People may mistake rosacea for acne, eczema or even the allergic skin reaction. Rosacea presents main symptoms including facial flushing, irritated skin, and pimples as well as other symptoms like blushing easily. It can often be clinically identified or with the help other instruments (e.g., dermatoscopy).
In some cases, clown nose-like lesions can serve as early indicators to genetic syndromes, including Hernandez syndrome and Tricho-Rhino-Phalangeal syndrome (31–33). This is of great clinical significance, because genetic syndromes with skin lesions and multisystemic involvement, including cancer predisposition, are often underrecognized. The majority of skin lesions are asymptomatic, easily leading to delayed diagnosis of underlying cancers in dermatological practice. We take Tricho-Rhino-Phalangeal syndrome as an example. It has three types, and its common manifestations include enlarged round nose, sparse hair, bone, and joint abnormalities (54). Unlike clown nose-like lesion caused by other causes, the nose in Tricho-Rhino-Phalangeal syndrome is usually enlarged into pear-shaped bulb and asymptomatic. More importantly, patients are often accompanied by impairments of other systems such as intellectual, musculoskeletal, and neurological systems. Dermatologists should have a systematic approach and recognize the characteristic clown nose-like lesion early, and render earlier genetic screening of patients and their family members.
Clown nose-like lesion was initially considered as a indicator of cutaneous metastatic malignancies, including lung carcinomas. Since most visceral malignant tumors have a poor prognosis, early diagnosis is very important. For older patients (usually more than 50 years old), careful consideration should be given to decide whether the asymptomatic clown nose-like lesion is a metastatic malignancy, especially when it appears for only a short period of time (within a few weeks). Detailed medical history, tissue biopsy, and systematic examination are necessary. The percentage of patients with cutaneous metastases originating from visceral cancers are ~0.7–9% (55), in which lung cancer metastasis happened in 1–12% of cases (2, 56). Metastatic transmission to the skin can occur in the following ways: lymphatic transmission, blood-borne transmission, direct continuity, and rarely iatrogenic implantation (57). Under most circumstances, the tumor will preferentially metastasize to the nearby skin, and distant metastasis to the skin is relatively rare (2). The mechanism of cancer metastasis to the nose has not been fully elucidated. As reported previously (58), tumor cells can be transported to the nose through the pulmonary blood vessels, lymphatic circulation, and vertebral venous plexus without any valves. In addition, an emboli traveling through the arteries was also a possible route of metastasis (59). Tumor emboli may enter the pulmonary vein, then the systemic circulation through the left atrium, and enter the cavernous body into the blood supply site. Another possible mechanism of nasal tip metastasis is that when the intrathoracic pressure increases significantly, blood-borne emboli drift upward through the venous plexus to the venous sinuses of the skull (20). However, the specific mechanism needs to be further clarified.
In this study, we comprehensively analyzed various causes of clown nose-like lesions from our clinical cases and published literatures to further guide clinical diagnosis. The causes of clown nose-like lesions may be metastatic visceral tumors, genetic syndromes, and primary diseases involving the nasal tip. Comprehensive evaluation of clown nose-like lesions (e.g., occurring time of clown nose-like lesion, the number/color/symptom of nodules or papules, gender preference, family history, genetic background, and concomitant systemic involvements) in combination with other clinical information (e.g., histopathological findings) is emphasized to narrow the diagnosis (Table 5). In conclusion, the term of clown nose-like lesion should be expanded to consider genetic syndromes and primary diseases that affect the nasal tip, in addition to cutaneous metastasis.
Table 5.
Identification points of clown nose-like lesions.
| Metastatic visceral tumors | Genetic syndromes | Primary nasal diseases | |
|---|---|---|---|
| Occurring time of clown nose-like lesion | Over 50 years old generally | Young age, even at birth | N/A |
| The number of nasal nodules or papules | Often solitary | Often multiple# | Solitary or multiple* |
| The color of nodules or papules | Often red or inflammatory | Often fresh-colored | Often red or inflammatory |
| The symptom of clown nose-like lesion | Asymptomatic | Asymptomatic | often tender or pruritic& |
| Gender | N/A, male preference | Female preference | N/A |
| Family history | None | Often positive | None |
| Genetic background | None | Positive | None |
| Accompanying involvements | Visceral tumors | Multiple system involvement | None |
| Prognosis | Poor | Depending on the other system(s) involved | N/A |
Except for some syndrome, e.g., Tricho-Rhino-Phalangeal Syndrome.
For nasal special infection, e.g., nasal leishmaniasis, nasal nodules are multiple.
There are individual differences in tender or pruritic sensations, and some clownlike nose can be asymptomatic.
“N/A,” data not available.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.
Ethics Statement
The studies involving human participants were reviewed and approved by Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital. Written informed consent to participate in this study was provided by the participants' legal guardian/next of kin. Written informed consent was obtained from the individual(s), and minor(s)' legal guardian/next of kin, for the publication of any potentially identifiable images or data included in this article.
Author Contributions
BZ contributed to literature search, data analysis, and drafting of the manuscript. LC contributed to conception of the study, case collection/analysis, literature search, and critical revision of the manuscript. JL and XL contributed to case collection/analysis. ZX contributed to case collection/analysis and constructive discussions. ZS contributed to conception and design of the study, literature search, data collection, and critical revision of the manuscript. All authors have approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would like to thank Dr. Xin Chen (China-Japan Friendship Hospital, Beijing, China), Dr. Ding Liu (Luoyang Central Hospital, Henan, China), and Dr. Lin Wang (West China Hospital of Sichuan University, Sichuan, China) for providing clinical cases with clown nose-like lesions.
Footnotes
Funding. This work was supported in part by clinical research and translation key project of Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital (No. 2016LZ02, ZS) and Sichuan Science and Technology Program (No. 2019JDTD0027, ZS).
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Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

